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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0005938 | cell cortex | 3 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
Related structures:
AlphaFold database: A4H562
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007015 | actin filament organization | 5 | 1 |
GO:0007163 | establishment or maintenance of cell polarity | 2 | 1 |
GO:0008360 | regulation of cell shape | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022603 | regulation of anatomical structure morphogenesis | 4 | 1 |
GO:0022604 | regulation of cell morphogenesis | 5 | 1 |
GO:0030865 | cortical cytoskeleton organization | 6 | 1 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 1 |
GO:0032970 | regulation of actin filament-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050793 | regulation of developmental process | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0005488 | binding | 1 | 4 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005525 | GTP binding | 5 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0019001 | guanyl nucleotide binding | 5 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0019900 | kinase binding | 4 | 1 |
GO:0019901 | protein kinase binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
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 | 0.532 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.247 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.281 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.407 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.450 |
CLV_PCSK_FUR_1 | 263 | 267 | PF00082 | 0.430 |
CLV_PCSK_FUR_1 | 572 | 576 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.567 |
DEG_MDM2_SWIB_1 | 181 | 189 | PF02201 | 0.392 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.308 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.317 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.408 |
DOC_MAPK_DCC_7 | 290 | 298 | PF00069 | 0.230 |
DOC_MAPK_gen_1 | 110 | 118 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 545 | 555 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.324 |
DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.184 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.392 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.372 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.394 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.300 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.241 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 388 | 393 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 548 | 553 | PF00244 | 0.341 |
LIG_Actin_WH2_2 | 196 | 211 | PF00022 | 0.307 |
LIG_APCC_ABBA_1 | 201 | 206 | PF00400 | 0.392 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.399 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.348 |
LIG_CSL_BTD_1 | 502 | 505 | PF09270 | 0.324 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.381 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.390 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.420 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.295 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.368 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.385 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.336 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.386 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.388 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.310 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.345 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 542 | 550 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 551 | 560 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 551 | 555 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.251 |
LIG_MAD2 | 112 | 120 | PF02301 | 0.388 |
LIG_MLH1_MIPbox_1 | 96 | 100 | PF16413 | 0.348 |
LIG_NRP_CendR_1 | 573 | 576 | PF00754 | 0.450 |
LIG_Pex14_1 | 32 | 36 | PF04695 | 0.325 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.327 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.391 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.285 |
LIG_REV1ctd_RIR_1 | 390 | 400 | PF16727 | 0.403 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.308 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.419 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.241 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 543 | 546 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.480 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.305 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.271 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 429 | 434 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 187 | 192 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 6 | 13 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.324 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.422 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.445 |
LIG_TYR_ITIM | 541 | 546 | PF00017 | 0.481 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.402 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.243 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.514 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.355 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.422 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.365 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.347 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.400 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.428 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.359 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.334 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.352 |
MOD_Cter_Amidation | 359 | 362 | PF01082 | 0.508 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.565 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.557 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.533 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.517 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.613 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.588 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.595 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.560 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.286 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.384 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.288 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.375 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.353 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.376 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.370 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.255 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.349 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.339 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.362 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.407 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.617 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.416 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.196 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.306 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.267 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.260 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.393 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.368 |
MOD_NEK2_2 | 448 | 453 | PF00069 | 0.409 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.341 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.229 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.314 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.236 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.318 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.333 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.341 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.347 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.402 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.342 |
MOD_Plk_2-3 | 517 | 523 | PF00069 | 0.419 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.351 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.219 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.392 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.357 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.404 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.482 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.298 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.264 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.355 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.298 |
MOD_SUMO_for_1 | 15 | 18 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 107 | 111 | PF00179 | 0.414 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.236 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.617 |
TRG_NES_CRM1_1 | 425 | 438 | PF08389 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.562 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT6 | Leptomonas seymouri | 70% | 100% |
A0A1X0NPJ9 | Trypanosomatidae | 47% | 100% |
A0A3R7KVN9 | Trypanosoma rangeli | 47% | 100% |
A0A3S5H622 | Leishmania donovani | 85% | 100% |
A4HTD9 | Leishmania infantum | 85% | 100% |
C9ZUH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ALD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q2UM43 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 91% |
Q4QIH3 | Leishmania major | 86% | 100% |
Q5B5L3 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 91% |
Q8RXF8 | Arabidopsis thaliana | 21% | 89% |
V5BTM0 | Trypanosoma cruzi | 46% | 100% |