Intracellular protein trafficking, Guanine nucleotide-binding beta subunit-like
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. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005840 | ribosome | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AH24
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.397 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.572 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 452 | 454 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.412 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.405 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.334 |
DEG_SPOP_SBC_1 | 505 | 509 | PF00917 | 0.552 |
DOC_CYCLIN_RxL_1 | 149 | 159 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 66 | 72 | PF00134 | 0.434 |
DOC_MAPK_DCC_7 | 312 | 322 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 151 | 157 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.378 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.405 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.538 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.425 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 290 | 298 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 65 | 69 | PF00244 | 0.439 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.469 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.332 |
LIG_Clathr_ClatBox_1 | 373 | 377 | PF01394 | 0.398 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.368 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.512 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.452 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.423 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.534 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.402 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.229 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.376 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.361 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.456 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.457 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.455 |
LIG_GBD_Chelix_1 | 58 | 66 | PF00786 | 0.458 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.364 |
LIG_PDZ_Class_2 | 550 | 555 | PF00595 | 0.505 |
LIG_REV1ctd_RIR_1 | 82 | 91 | PF16727 | 0.359 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.309 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.484 |
LIG_SH2_GRB2like | 313 | 316 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.472 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 74 | 81 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 153 | 159 | PF11976 | 0.440 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.407 |
LIG_WRC_WIRS_1 | 550 | 555 | PF05994 | 0.540 |
MOD_CDC14_SPxK_1 | 230 | 233 | PF00782 | 0.507 |
MOD_CDK_SPxK_1 | 227 | 233 | PF00069 | 0.475 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.464 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.496 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.395 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.491 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.381 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.368 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.499 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.537 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.408 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.360 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.451 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.442 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.420 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.465 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.436 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.367 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.590 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.544 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.455 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.231 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.354 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.473 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.344 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.442 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.445 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.195 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.355 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.325 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.374 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.527 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.439 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.383 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.514 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.416 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.536 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.480 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.373 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.518 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.423 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.466 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.491 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.396 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.432 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.458 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.330 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.530 |
MOD_NEK2_2 | 441 | 446 | PF00069 | 0.272 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.389 |
MOD_PKA_1 | 239 | 245 | PF00069 | 0.437 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.390 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.504 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.444 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.431 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.373 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.361 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.275 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.508 |
MOD_Plk_2-3 | 537 | 543 | PF00069 | 0.339 |
MOD_Plk_2-3 | 549 | 555 | PF00069 | 0.476 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.484 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.419 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.469 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.363 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.535 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.347 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.423 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.512 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.276 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.505 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.484 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.565 |
MOD_SUMO_rev_2 | 108 | 112 | PF00179 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1S8 | Leptomonas seymouri | 73% | 100% |
A0A1X0NIQ5 | Trypanosomatidae | 48% | 99% |
A0A3R7NVJ1 | Trypanosoma rangeli | 47% | 99% |
A0A3S7WY01 | Leishmania donovani | 100% | 100% |
A4HD70 | Leishmania braziliensis | 91% | 100% |
C9ZSK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 87% |
D0A6Y3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 99% |
E9AWK2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4QAW8 | Leishmania major | 98% | 100% |
V5C0S8 | Trypanosoma cruzi | 48% | 99% |