Intracellular protein trafficking, GTPase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HSG8
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.691 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.164 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.204 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.239 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.239 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.227 |
CLV_PCSK_PC1ET2_1 | 591 | 593 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 587 | 593 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.382 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.239 |
DOC_CYCLIN_RxL_1 | 6 | 16 | PF00134 | 0.573 |
DOC_MAPK_gen_1 | 100 | 109 | PF00069 | 0.239 |
DOC_MAPK_gen_1 | 110 | 118 | PF00069 | 0.239 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.239 |
DOC_MAPK_gen_1 | 242 | 253 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 313 | 323 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 424 | 432 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.239 |
DOC_MAPK_MEF2A_6 | 274 | 281 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 314 | 323 | PF00069 | 0.347 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.515 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.352 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 142 | 146 | PF12436 | 0.239 |
DOC_USP7_UBL2_3 | 182 | 186 | PF12436 | 0.639 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.551 |
DOC_USP7_UBL2_3 | 341 | 345 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.384 |
DOC_USP7_UBL2_3 | 438 | 442 | PF12436 | 0.353 |
DOC_USP7_UBL2_3 | 593 | 597 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 20 | 24 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 339 | 344 | PF00244 | 0.447 |
LIG_CaM_NSCaTE_8 | 618 | 625 | PF13499 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 132 | 139 | PF00928 | 0.243 |
LIG_deltaCOP1_diTrp_1 | 425 | 432 | PF00928 | 0.330 |
LIG_deltaCOP1_diTrp_1 | 461 | 469 | PF00928 | 0.318 |
LIG_deltaCOP1_diTrp_1 | 614 | 621 | PF00928 | 0.435 |
LIG_eIF4E_1 | 247 | 253 | PF01652 | 0.427 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.404 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.310 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.318 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.433 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.630 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.239 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.266 |
LIG_Integrin_RGD_1 | 511 | 513 | PF01839 | 0.674 |
LIG_LIR_Gen_1 | 103 | 109 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 265 | 276 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 353 | 361 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 497 | 505 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 615 | 625 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 497 | 502 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.430 |
LIG_LYPXL_yS_3 | 276 | 279 | PF13949 | 0.269 |
LIG_LYPXL_yS_3 | 326 | 329 | PF13949 | 0.404 |
LIG_PCNA_yPIPBox_3 | 377 | 391 | PF02747 | 0.404 |
LIG_Pex14_1 | 135 | 139 | PF04695 | 0.239 |
LIG_Pex14_1 | 207 | 211 | PF04695 | 0.299 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.465 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.239 |
LIG_SH2_GRB2like | 168 | 171 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 358 | 361 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.239 |
LIG_SH2_STAT3 | 460 | 463 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.497 |
LIG_SH3_2 | 15 | 20 | PF14604 | 0.499 |
LIG_SH3_2 | 551 | 556 | PF14604 | 0.564 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.611 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.337 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.695 |
LIG_SH3_4 | 3 | 10 | PF00018 | 0.555 |
LIG_SUMO_SIM_par_1 | 114 | 121 | PF11976 | 0.239 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.564 |
LIG_TRAF2_1 | 624 | 627 | PF00917 | 0.366 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.404 |
LIG_UBA3_1 | 334 | 341 | PF00899 | 0.408 |
LIG_WRC_WIRS_1 | 499 | 504 | PF05994 | 0.406 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.532 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.531 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.241 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.744 |
MOD_Cter_Amidation | 4 | 7 | PF01082 | 0.552 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.413 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.751 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.650 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.323 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.449 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.408 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.407 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.571 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.575 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.396 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.262 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.264 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.312 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.415 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.415 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.239 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.239 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.692 |
MOD_PK_1 | 339 | 345 | PF00069 | 0.447 |
MOD_PKA_1 | 339 | 345 | PF00069 | 0.447 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.619 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.449 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.446 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.415 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.477 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.249 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.254 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.570 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.630 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.771 |
MOD_Plk_2-3 | 523 | 529 | PF00069 | 0.677 |
MOD_Plk_2-3 | 537 | 543 | PF00069 | 0.533 |
MOD_Plk_2-3 | 610 | 616 | PF00069 | 0.601 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.239 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.239 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.404 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.307 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.239 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.437 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.375 |
MOD_SUMO_rev_2 | 117 | 125 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 187 | 192 | PF00179 | 0.484 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.362 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.239 |
TRG_NES_CRM1_1 | 382 | 394 | PF08389 | 0.419 |
TRG_NLS_Bipartite_1 | 130 | 150 | PF00514 | 0.384 |
TRG_NLS_Bipartite_1 | 20 | 40 | PF00514 | 0.449 |
TRG_NLS_MonoExtC_3 | 144 | 149 | PF00514 | 0.239 |
TRG_NLS_MonoExtC_3 | 583 | 588 | PF00514 | 0.387 |
TRG_NLS_MonoExtN_4 | 142 | 149 | PF00514 | 0.239 |
TRG_NLS_MonoExtN_4 | 310 | 317 | PF00514 | 0.455 |
TRG_NLS_MonoExtN_4 | 33 | 40 | PF00514 | 0.400 |
TRG_NLS_MonoExtN_4 | 582 | 588 | PF00514 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.239 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P303 | Leptomonas seymouri | 83% | 100% |
A0A0S4JVL9 | Bodo saltans | 67% | 100% |
A0A1X0NJV6 | Trypanosomatidae | 71% | 100% |
A0A3S5H5H9 | Leishmania donovani | 100% | 100% |
A0A422N2R2 | Trypanosoma rangeli | 70% | 100% |
A2XGQ1 | Oryza sativa subsp. indica | 51% | 100% |
A4H492 | Leishmania braziliensis | 87% | 100% |
C9ZUE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AKF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
J9VQ03 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 47% | 87% |
O14236 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 48% | 100% |
P0CS94 | Cryptococcus neoformans var. grubii | 46% | 90% |
P53742 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 46% | 100% |
Q10LF7 | Oryza sativa subsp. japonica | 51% | 100% |
Q13823 | Homo sapiens | 47% | 86% |
Q4QJF6 | Leishmania major | 96% | 100% |
Q6C036 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 45% | 100% |
Q6CSP9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 45% | 100% |
Q6FWS1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 46% | 100% |
Q6TGJ8 | Cryptococcus gattii | 45% | 86% |
Q75DA4 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 47% | 100% |
Q7SHR8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 44% | 100% |
Q99LH1 | Mus musculus | 52% | 86% |
Q9C3Z4 | Pneumocystis carinii | 44% | 100% |
Q9C923 | Arabidopsis thaliana | 51% | 100% |
Q9SJF1 | Arabidopsis thaliana | 27% | 100% |
V5BAQ6 | Trypanosoma cruzi | 68% | 100% |