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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AIL1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0043085 | positive regulation of catalytic activity | 4 | 7 |
GO:0043087 | regulation of GTPase activity | 5 | 7 |
GO:0043547 | positive regulation of GTPase activity | 6 | 7 |
GO:0044093 | positive regulation of molecular function | 3 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051336 | regulation of hydrolase activity | 4 | 7 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 7 |
GO:0008047 | enzyme activator activity | 3 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 7 |
GO:0030695 | GTPase regulator activity | 4 | 7 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 7 |
GO:0098772 | molecular function regulator activity | 1 | 7 |
GO:0140677 | molecular function activator activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.822 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.304 |
CLV_PCSK_FUR_1 | 307 | 311 | PF00082 | 0.418 |
CLV_PCSK_FUR_1 | 518 | 522 | PF00082 | 0.376 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 249 | 255 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.349 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.581 |
DOC_CYCLIN_RxL_1 | 257 | 269 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 253 | 263 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 493 | 501 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 370 | 382 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 410 | 417 | PF00069 | 0.680 |
DOC_PP1_RVXF_1 | 397 | 404 | PF00149 | 0.463 |
DOC_PP1_RVXF_1 | 498 | 504 | PF00149 | 0.539 |
DOC_PP1_RVXF_1 | 518 | 525 | PF00149 | 0.572 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.860 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.754 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.857 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 317 | 324 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 521 | 529 | PF00244 | 0.244 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.546 |
LIG_CaM_IQ_9 | 40 | 55 | PF13499 | 0.685 |
LIG_eIF4E_1 | 389 | 395 | PF01652 | 0.530 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.427 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.538 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.539 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.628 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.642 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.427 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.478 |
LIG_IRF3_LxIS_1 | 390 | 397 | PF10401 | 0.427 |
LIG_LIR_Apic_2 | 218 | 223 | PF02991 | 0.746 |
LIG_LIR_Apic_2 | 509 | 513 | PF02991 | 0.681 |
LIG_LIR_Apic_2 | 70 | 75 | PF02991 | 0.777 |
LIG_LIR_Gen_1 | 342 | 348 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 376 | 382 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.754 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.584 |
LIG_MYND_1 | 136 | 140 | PF01753 | 0.829 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.546 |
LIG_Rb_pABgroove_1 | 369 | 377 | PF01858 | 0.546 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.546 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.618 |
LIG_SH2_STAT3 | 463 | 466 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.620 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.779 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.715 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.427 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 366 | 372 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 423 | 431 | PF11976 | 0.671 |
LIG_SUMO_SIM_par_1 | 294 | 301 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.530 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.501 |
LIG_TRFH_1 | 285 | 289 | PF08558 | 0.546 |
LIG_UBA3_1 | 402 | 410 | PF00899 | 0.585 |
LIG_WRC_WIRS_1 | 69 | 74 | PF05994 | 0.782 |
LIG_WW_3 | 139 | 143 | PF00397 | 0.829 |
MOD_CDC14_SPxK_1 | 139 | 142 | PF00782 | 0.667 |
MOD_CDC14_SPxK_1 | 512 | 515 | PF00782 | 0.674 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.668 |
MOD_CDK_SPxK_1 | 509 | 515 | PF00069 | 0.660 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.743 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.789 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.576 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.813 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.679 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.649 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.526 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.427 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.557 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.547 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.485 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.569 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.531 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.556 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.332 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.346 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.409 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.607 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.509 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.768 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.704 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.746 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.618 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.725 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.580 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.643 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.673 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.741 |
MOD_LATS_1 | 58 | 64 | PF00433 | 0.785 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.460 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.626 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.532 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.779 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.649 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.708 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.721 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.448 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.546 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.383 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.538 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.648 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.408 |
MOD_NEK2_2 | 513 | 518 | PF00069 | 0.589 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.730 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.538 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.551 |
MOD_PKA_1 | 309 | 315 | PF00069 | 0.546 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.800 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.562 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.527 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.699 |
MOD_PKB_1 | 132 | 140 | PF00069 | 0.787 |
MOD_PKB_1 | 172 | 180 | PF00069 | 0.732 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.814 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.546 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.699 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.491 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.686 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.546 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.722 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.474 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.618 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.487 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.500 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.274 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.707 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.742 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.669 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.630 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.824 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.546 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.660 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.747 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.707 |
MOD_SUMO_rev_2 | 404 | 412 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 80 | 89 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_2 | 473 | 479 | PF01217 | 0.617 |
TRG_DiLeu_BaEn_4 | 474 | 480 | PF01217 | 0.617 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 497 | 502 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 171 | 174 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.661 |
TRG_ER_FFAT_2 | 66 | 78 | PF00635 | 0.659 |
TRG_NES_CRM1_1 | 369 | 383 | PF08389 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P406 | Leptomonas seymouri | 54% | 93% |
A0A3S7WWA9 | Leishmania donovani | 75% | 91% |
A4HYZ3 | Leishmania infantum | 76% | 91% |
E9AUU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 91% |
Q4QCN9 | Leishmania major | 75% | 100% |