Homologous to other Eukaryotic mitochondrial outer membrane GTPases.. The lone C-terminal TM segment has a high positive charge at both ends, characteristic of mitochondrial outer membrane anchored proteins.. Localization: Mitochondrial (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0005938 | cell cortex | 3 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0031410 | cytoplasmic vesicle | 6 | 2 |
GO:0031982 | vesicle | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0097708 | intracellular vesicle | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QIH3
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007015 | actin filament organization | 5 | 2 |
GO:0007163 | establishment or maintenance of cell polarity | 2 | 2 |
GO:0008360 | regulation of cell shape | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022603 | regulation of anatomical structure morphogenesis | 4 | 2 |
GO:0022604 | regulation of cell morphogenesis | 5 | 2 |
GO:0030865 | cortical cytoskeleton organization | 6 | 2 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 2 |
GO:0032970 | regulation of actin filament-based process | 4 | 2 |
GO:0033043 | regulation of organelle organization | 5 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050793 | regulation of developmental process | 3 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003924 | GTPase activity | 7 | 2 |
GO:0005488 | binding | 1 | 5 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005525 | GTP binding | 5 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0019001 | guanyl nucleotide binding | 5 | 2 |
GO:0019899 | enzyme binding | 3 | 2 |
GO:0019900 | kinase binding | 4 | 2 |
GO:0019901 | protein kinase binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:0005509 | calcium ion binding | 5 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 371 | 375 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.461 |
CLV_PCSK_FUR_1 | 572 | 576 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.565 |
DEG_MDM2_SWIB_1 | 181 | 189 | PF02201 | 0.390 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.309 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.316 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.414 |
DOC_CDC14_PxL_1 | 154 | 162 | PF14671 | 0.363 |
DOC_MAPK_gen_1 | 110 | 118 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 545 | 555 | PF00069 | 0.261 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.326 |
DOC_MAPK_MEF2A_6 | 289 | 298 | PF00069 | 0.329 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.390 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.319 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.372 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 289 | 296 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 388 | 393 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 548 | 553 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 562 | 568 | PF00244 | 0.426 |
LIG_APCC_ABBA_1 | 201 | 206 | PF00400 | 0.392 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.396 |
LIG_BIR_III_4 | 150 | 154 | PF00653 | 0.378 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.409 |
LIG_CSL_BTD_1 | 502 | 505 | PF09270 | 0.319 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.376 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.413 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.300 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.366 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.389 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.334 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.378 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.319 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.350 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 451 | 461 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 542 | 550 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 551 | 560 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 551 | 555 | PF02991 | 0.292 |
LIG_MAD2 | 112 | 120 | PF02301 | 0.389 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.328 |
LIG_NRP_CendR_1 | 573 | 576 | PF00754 | 0.467 |
LIG_Pex14_1 | 32 | 36 | PF04695 | 0.324 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.326 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.388 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.278 |
LIG_REV1ctd_RIR_1 | 390 | 400 | PF16727 | 0.398 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.309 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 543 | 546 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.276 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.506 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.306 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 429 | 434 | PF11976 | 0.290 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 6 | 13 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.325 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.423 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.451 |
LIG_TYR_ITIM | 541 | 546 | PF00017 | 0.494 |
LIG_UBA3_1 | 59 | 64 | PF00899 | 0.239 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.403 |
MOD_CDK_SPxxK_3 | 65 | 72 | PF00069 | 0.387 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.353 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.417 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.243 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.333 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.435 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.366 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.369 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.349 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.339 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.344 |
MOD_Cter_Amidation | 359 | 362 | PF01082 | 0.509 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.561 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.704 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.516 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.608 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.593 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.599 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.405 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.383 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.282 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.368 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.352 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.370 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.294 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.365 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.342 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.406 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.616 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.494 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.413 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.380 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.196 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.302 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.327 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.378 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.259 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.426 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.402 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.362 |
MOD_NEK2_2 | 448 | 453 | PF00069 | 0.409 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.341 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.307 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.256 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.318 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.334 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.341 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.401 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.341 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.374 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.296 |
MOD_Plk_2-3 | 517 | 523 | PF00069 | 0.424 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.348 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.212 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.396 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.356 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.404 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.468 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.262 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.329 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.356 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.326 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.300 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.326 |
MOD_SUMO_rev_2 | 107 | 111 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.637 |
TRG_NES_CRM1_1 | 425 | 438 | PF08389 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT6 | Leptomonas seymouri | 69% | 100% |
A0A1X0NPJ9 | Trypanosomatidae | 45% | 100% |
A0A3R7KVN9 | Trypanosoma rangeli | 47% | 100% |
A0A3S5H622 | Leishmania donovani | 93% | 100% |
A4H562 | Leishmania braziliensis | 86% | 100% |
A4HTD9 | Leishmania infantum | 93% | 100% |
C9ZUH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ALD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P0CO78 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 21% | 84% |
P0CO79 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 21% | 84% |
Q2UM43 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 91% |
Q4WN24 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 22% | 91% |
Q5B5L3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 91% |
Q8RXF8 | Arabidopsis thaliana | 21% | 89% |
V5BTM0 | Trypanosoma cruzi | 46% | 100% |