Proteopedia - User contributions [en]

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:47:46Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1bo4' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

''This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.''

<scene name='11/1107934/Rainbow/1'> 5'N to 3'C rainbow colouring of Protein</scene>

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

''This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.''

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:47:02Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1bo4' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

''This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.''

<scene name='11/1107934/Rainbow/1'> 5'N to #'C rainbow colouring of Protein</scene>

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

''This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.''

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:38:56Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1bo4' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

''This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.''

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

''This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.''

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:35:44Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

''This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.''

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

''This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.''

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:35:19Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

''This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.''

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:34:54Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

<ref name= "Wolf"> PMID 9727487</ref>
<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:32:53Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

<ref name= "Ransey">PMID:28504306</ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:32:11Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

<ref name= "Ransey">PMID:28504306(/ref>
</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:31:30Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]

<ref name= "Ransey">PMID:28504306(/ref>
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:26:38Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'> Site of catalysis</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:24:51Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/1'>N 5' to 3' C Rainbow Spectral colour coding</scene>

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:21:21Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' Catalytic Residues=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:20:15Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

<scene name='11/1107934/Catalytic_residues/3'>Acetyl CoA and Catalytic Acids Arg118 and Arg119</scene>
==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:17:18Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:17:03Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>

Aminoglycoside Acetlytransferases were first identified in Serratia marcescens in the 1960s and later crystallized in 1998, revealing key details about the structure and function of acetyltransferases. S. marcescens is a gram-negative bacteria that is known to cause UTIs, pneumonia, and sepsis. Aminoglycoside antibiotics, such as Sisomicin are used to treat these conditions by inactivating the bacterias’ ribosome. Antibiotic resistance and the growing danger of superbugs among bacterial infections combined with the lack of new antibiotic developments, indicates a need to better understand how proteins that confer antibiotic resistance to bacteria can circumvent our current treatment options.

This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:15:48Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>Spermidine and Catalytic Base Asp147</scene>

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:15:16Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

<scene name='11/1107934/Catalytic_residues/2'>TextToBeDisplayed</scene>

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T16:03:52Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='Catalytic Residues' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T15:34:47Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1bo4' size='340' side='right' caption='Aminoglycoside Acetyltransferase Dimer in Serratia Marcescens' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T15:33:34Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1bo4' size='340' side='right' caption='Caption for this structure' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T14:24:31Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====

[[Image:Butterfly AAC colour coded.png |400p px|left|thumb|Figure 1. The coolest image of this protein EVAH!!!]] ‎

== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
[[https://proteopedia.org/w/1bo4|CRYSTAL STRUCTURE OF A GCN5-RELATED N-ACETYLTRANSFERASE: SERRATIA MARESCENS AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE]]
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

File:Butterfly AAC colour coded.png

2026-04-24T14:11:43Z

Aleena Ahmad: The dimer structure of SmAAC illustrated with each motif colour coded

== Summary ==
The dimer structure of SmAAC illustrated with each motif colour coded

User:Aleena Ahmad/Sandbox 1

2026-04-24T13:44:47Z

Aleena Ahmad:

=='''Aminoglycoside Acetyltransferase in ''Serratia Marcescens'''''==
<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

==Introduction==
===GNAT Superfamily===
====Conserved Motifs====
== Function ==

==Mechanism==

== Structures of Importance==
===C-terminal===
===Possible Catalytic Residues===
===Importance of Dimer===

== Disease ==

== Relevance ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
<references/>

==Student Contributors===
*Aleena Ahmad
*Brynn Mitchell
*Jessica Paulson

User:Aleena Ahmad/Sandbox 1

2026-04-24T13:36:20Z

Aleena Ahmad:

User:Aleena Ahmad/Sandbox 1

2026-04-21T20:01:58Z

Aleena Ahmad: Created page with "==Your Heading Here (maybe something like 'Structure')== <StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''> This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:..."

==Your Heading Here (maybe something like 'Structure')==
<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
This is a default text for your page '''Aleena Ahmad/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.

== Function ==

== Disease ==

== Relevance ==

== Structural highlights ==

This is a sample scene created with SAT to <scene name='10/1070530/1stp_coloerd/1'>color</scene> by Group, and another to make <scene name='10/1070530/1stp_transparency/1'>a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>
== References ==
<references/>

User:Aleena Ahmad

2026-04-21T19:22:26Z

Aleena Ahmad:

* Full Real Name: Aleena Ahmad

* Position: Student

* Institution (NO ABBREVIATIONS): Butler University

* City, State/Province: Indianapolis

* Country: United States

* Field of Expertise or Study: Biochemistry

* ORCID ID:
*[[User:Aleena Ahmad/Sandbox 1]]
(ORCID, the Open Researcher and Contributor ID, is a free, unique, persistent identifier https://orcid.org)