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 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCN9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
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:0046907 | intracellular transport | 3 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
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:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
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 | 205 | 209 | PF00656 | 0.827 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.410 |
CLV_PCSK_FUR_1 | 359 | 363 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 301 | 307 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 192 | 196 | PF03568 | 0.812 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.773 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.574 |
DOC_ANK_TNKS_1 | 71 | 78 | PF00023 | 0.578 |
DOC_CYCLIN_RxL_1 | 309 | 321 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 567 | 578 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 305 | 315 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 462 | 469 | PF00069 | 0.689 |
DOC_PP1_RVXF_1 | 570 | 577 | PF00149 | 0.572 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.861 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.776 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.663 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 520 | 524 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 78 | 87 | PF00244 | 0.667 |
LIG_Actin_WH2_2 | 229 | 247 | PF00022 | 0.635 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.546 |
LIG_CaM_IQ_9 | 92 | 107 | PF13499 | 0.679 |
LIG_Clathr_ClatBox_1 | 431 | 435 | PF01394 | 0.486 |
LIG_EH1_1 | 375 | 383 | PF00400 | 0.574 |
LIG_eIF4E_1 | 441 | 447 | PF01652 | 0.530 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.808 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.546 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.539 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.406 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.574 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.609 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.501 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 561 | 565 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 343 | 351 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.590 |
LIG_LIR_LC3C_4 | 443 | 448 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.589 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.827 |
LIG_NRBOX | 312 | 318 | PF00104 | 0.546 |
LIG_NRBOX | 504 | 510 | PF00104 | 0.585 |
LIG_Rb_LxCxE_1 | 27 | 46 | PF01857 | 0.632 |
LIG_Rb_pABgroove_1 | 421 | 429 | PF01858 | 0.546 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.531 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.580 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.625 |
LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.632 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.644 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.843 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.782 |
LIG_SUMO_SIM_anti_2 | 418 | 424 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 475 | 483 | PF11976 | 0.672 |
LIG_SUMO_SIM_par_1 | 346 | 353 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 430 | 435 | PF11976 | 0.530 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.640 |
LIG_TRFH_1 | 337 | 341 | PF08558 | 0.411 |
LIG_UBA3_1 | 454 | 462 | PF00899 | 0.473 |
LIG_WW_3 | 192 | 196 | PF00397 | 0.804 |
MOD_CDC14_SPxK_1 | 564 | 567 | PF00782 | 0.598 |
MOD_CDK_SPxK_1 | 561 | 567 | PF00069 | 0.580 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.778 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.784 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.735 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.759 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.512 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.450 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.394 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.741 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.493 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.689 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.438 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.369 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.370 |
MOD_Cter_Amidation | 76 | 79 | PF01082 | 0.492 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.736 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.698 |
MOD_GlcNHglycan | 153 | 157 | PF01048 | 0.771 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.705 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.430 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.411 |
MOD_GlcNHglycan | 435 | 439 | PF01048 | 0.500 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.629 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.659 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.808 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.705 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.683 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.475 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.748 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.471 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.312 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.458 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.370 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.541 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.595 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.667 |
MOD_LATS_1 | 110 | 116 | PF00433 | 0.709 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.740 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.790 |
MOD_N-GLC_2 | 49 | 51 | PF02516 | 0.367 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.748 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.653 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.658 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.411 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.350 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.496 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.415 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.728 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.770 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.401 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.372 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.585 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.676 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.740 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.433 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.380 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.602 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.585 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.747 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.690 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.770 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.411 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.711 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.411 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.654 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.512 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.339 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.744 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.657 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.793 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.359 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.580 |
MOD_SUMO_for_1 | 461 | 464 | PF00179 | 0.436 |
MOD_SUMO_for_1 | 566 | 569 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 26 | 31 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_2 | 525 | 531 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_4 | 526 | 532 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.593 |
TRG_NES_CRM1_1 | 421 | 435 | PF08389 | 0.512 |
TRG_NLS_Bipartite_1 | 64 | 82 | PF00514 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P406 | Leptomonas seymouri | 55% | 100% |
A0A3S7WWA9 | Leishmania donovani | 93% | 100% |
A4HYZ3 | Leishmania infantum | 93% | 100% |
E9AIL1 | Leishmania braziliensis | 75% | 100% |
E9AUU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |