P9WGP5
Gene name |
secA1 |
Protein name |
Protein translocase subunit SecA 1 |
Names |
tbSecA |
Species |
Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) |
KEGG Pathway |
mtu:Rv3240c |
EC number |
7.4.2.8: Linked to the hydrolysis of a nucleoside triphosphate |
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
3 structures for P9WGP5
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 1NKT | X-ray | 260 A | A/B | 2-892 | PDB |
| 1NL3 | X-ray | 280 A | A/B | 2-892 | PDB |
| AF-P9WGP5-F1 | Predicted | AlphaFoldDB |
No variants for P9WGP5
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for P9WGP5 | |||||
No associated diseases with P9WGP5
8 regional properties for P9WGP5
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Helicase, C-terminal | 419 - 620 | IPR001650 |
| domain | SecA DEAD-like, N-terminal | 2 - 383 | IPR011115 |
| domain | SecA Wing/Scaffold | 613 - 833 | IPR011116 |
| domain | SecA, preprotein cross-linking domain | 227 - 339 | IPR011130 |
| domain | Helicase superfamily 1/2, ATP-binding domain | 88 - 246 | IPR014001 |
| domain | SecA motor DEAD | 1 - 615 | IPR014018 |
| conserved_site | SecA conserved site | 481 - 496 | IPR020937 |
| domain | SecA, C-terminal helicase domain | 401 - 585 | IPR044722 |
Functions
| Description | ||
|---|---|---|
| EC Number | 7.4.2.8 | Linked to the hydrolysis of a nucleoside triphosphate |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
6 GO annotations of cellular component
| Name | Definition |
|---|---|
| cell envelope Sec protein transport complex | A transmembrane protein complex involved in the translocation of proteins across the cytoplasmic membrane. In Gram-negative bacteria, Sec-translocated proteins are subsequently secreted via the type II, IV, or V secretion systems. Sec complex components include SecA, D, E, F, G, Y and YajC. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| extracellular region | The space external to the outermost structure of a cell. For cells without external protective or external encapsulating structures this refers to space outside of the plasma membrane. This term covers the host cell environment outside an intracellular parasite. |
| integral component of plasma membrane | The component of the plasma membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane. |
| peptidoglycan-based cell wall | A protective structure outside the cytoplasmic membrane composed of peptidoglycan (also known as murein), a molecule made up of a glycan (sugar) backbone of repetitively alternating N-acetylglucosamine and N-acetylmuramic acid with short, attached, cross-linked peptide chains containing unusual amino acids. An example of this component is found in Escherichia coli. |
| plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
4 GO annotations of molecular function
| Name | Definition |
|---|---|
| ABC-type protein transporter activity | Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + protein(out) = ADP + phosphate + protein(in). |
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| ATP hydrolysis activity | Catalysis of the reaction: ATP + H2O = ADP + H+ phosphate. ATP hydrolysis is used in some reactions as an energy source, for example to catalyze a reaction or drive transport against a concentration gradient. |
| protein-exporting ATPase activity | Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + protein+(in) -> ADP + phosphate + protein+(out); drives the concomitant secretion of proteins. |
4 GO annotations of biological process
| Name | Definition |
|---|---|
| intracellular protein transmembrane transport | The directed movement of proteins in a cell, from one side of a membrane to another by means of some agent such as a transporter or pore. |
| protein import | The targeting and directed movement of proteins into a cell or organelle. Not all import involves an initial targeting event. |
| protein targeting | The process of targeting specific proteins to particular regions of the cell, typically membrane-bounded subcellular organelles. Usually requires an organelle specific protein sequence motif. |
| protein transport by the Sec complex | The process in which unfolded proteins are transported across the cytoplasmic membrane in Gram-positive and Gram-negative bacteria by the Sec complex, in a process involving proteolytic cleavage of an N-terminal signal peptide. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MLSKLLRLGE | GRMVKRLKKV | ADYVGTLSDD | VEKLTDAELR | AKTDEFKRRL | ADQKNPETLD |
| 70 | 80 | 90 | 100 | 110 | 120 |
| DLLPEAFAVA | REAAWRVLDQ | RPFDVQVMGA | AALHLGNVAE | MKTGEGKTLT | CVLPAYLNAL |
| 130 | 140 | 150 | 160 | 170 | 180 |
| AGNGVHIVTV | NDYLAKRDSE | WMGRVHRFLG | LQVGVILATM | TPDERRVAYN | ADITYGTNNE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| FGFDYLRDNM | AHSLDDLVQR | GHHYAIVDEV | DSILIDEART | PLIISGPADG | ASNWYTEFAR |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LAPLMEKDVH | YEVDLRKRTV | GVHEKGVEFV | EDQLGIDNLY | EAANSPLVSY | LNNALKAKEL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| FSRDKDYIVR | DGEVLIVDEF | TGRVLIGRRY | NEGMHQAIEA | KEHVEIKAEN | QTLATITLQN |
| 370 | 380 | 390 | 400 | 410 | 420 |
| YFRLYDKLAG | MTGTAQTEAA | ELHEIYKLGV | VSIPTNMPMI | REDQSDLIYK | TEEAKYIAVV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| DDVAERYAKG | QPVLIGTTSV | ERSEYLSRQF | TKRRIPHNVL | NAKYHEQEAT | IIAVAGRRGG |
| 490 | 500 | 510 | 520 | 530 | 540 |
| VTVATNMAGR | GTDIVLGGNV | DFLTDQRLRE | RGLDPVETPE | EYEAAWHSEL | PIVKEEASKE |
| 550 | 560 | 570 | 580 | 590 | 600 |
| AKEVIEAGGL | YVLGTERHES | RRIDNQLRGR | SGRQGDPGES | RFYLSLGDEL | MRRFNGAALE |
| 610 | 620 | 630 | 640 | 650 | 660 |
| TLLTRLNLPD | DVPIEAKMVT | RAIKSAQTQV | EQQNFEVRKN | VLKYDEVMNQ | QRKVIYAERR |
| 670 | 680 | 690 | 700 | 710 | 720 |
| RILEGENLKD | QALDMVRDVI | TAYVDGATGE | GYAEDWDLDA | LWTALKTLYP | VGITADSLTR |
| 730 | 740 | 750 | 760 | 770 | 780 |
| KDHEFERDDL | TREELLEALL | KDAERAYAAR | EAELEEIAGE | GAMRQLERNV | LLNVIDRKWR |
| 790 | 800 | 810 | 820 | 830 | 840 |
| EHLYEMDYLK | EGIGLRAMAQ | RDPLVEYQRE | GYDMFMAMLD | GMKEESVGFL | FNVTVEAVPA |
| 850 | 860 | 870 | 880 | 890 | 900 |
| PPVAPAAEPA | ELAEFAAAAA | AAAQQRSAVD | GGARERAPSA | LRAKGVASES | PALTYSGPAE |
| 910 | 920 | 930 | 940 | ||
| DGSAQVQRNG | GGAHKTPAGV | PAGASRRERR | EAARRQGRGA | KPPKSVKKR |