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 |
Related structures:
AlphaFold database: Q4Q0T3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.527 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.420 |
DEG_ODPH_VHL_1 | 4 | 17 | PF01847 | 0.598 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.620 |
DOC_MAPK_gen_1 | 7 | 17 | PF00069 | 0.574 |
DOC_MAPK_JIP1_4 | 407 | 413 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 46 | 53 | PF00069 | 0.427 |
DOC_MAPK_NFAT4_5 | 46 | 54 | PF00069 | 0.435 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 212 | 217 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 443 | 451 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 8 | 17 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 86 | 90 | PF00244 | 0.501 |
LIG_14-3-3_CterR_2 | 507 | 511 | PF00244 | 0.365 |
LIG_Actin_WH2_2 | 190 | 206 | PF00022 | 0.332 |
LIG_Actin_WH2_2 | 76 | 94 | PF00022 | 0.366 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.553 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.538 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.439 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.459 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.328 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.542 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.622 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.534 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.553 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.579 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.412 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.349 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.363 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.662 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.359 |
LIG_LIR_Apic_2 | 112 | 116 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.403 |
LIG_MYND_1 | 2 | 6 | PF01753 | 0.615 |
LIG_Pex14_1 | 486 | 490 | PF04695 | 0.325 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.410 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.521 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.394 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.317 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.422 |
LIG_SH2_NCK_1 | 113 | 117 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.389 |
LIG_SH3_1 | 103 | 109 | PF00018 | 0.586 |
LIG_SH3_2 | 3 | 8 | PF14604 | 0.609 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.514 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.444 |
LIG_SUMO_SIM_par_1 | 224 | 240 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 329 | 336 | PF11976 | 0.353 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.606 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.388 |
LIG_TYR_ITSM | 373 | 380 | PF00017 | 0.345 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.324 |
LIG_WW_3 | 107 | 111 | PF00397 | 0.657 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.451 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.394 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.625 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.556 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.503 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.340 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.652 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.589 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.588 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.753 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.378 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.680 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.471 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.499 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.310 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.426 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.577 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.345 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.609 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.609 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.360 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.352 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.504 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.647 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.406 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.510 |
MOD_PKA_1 | 23 | 29 | PF00069 | 0.489 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.512 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.564 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.652 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.525 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.473 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.590 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.386 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.495 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.560 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.580 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.451 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.340 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.364 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.353 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.427 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.222 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.361 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.409 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 13 | 17 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 353 | 358 | PF00179 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.321 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.338 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.571 |
TRG_NES_CRM1_1 | 217 | 232 | PF08389 | 0.341 |
TRG_NLS_Bipartite_1 | 7 | 25 | PF00514 | 0.546 |
TRG_NLS_MonoCore_2 | 20 | 25 | PF00514 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDJ0 | Leptomonas seymouri | 57% | 100% |
A0A3S7XBN4 | Leishmania donovani | 92% | 100% |
A4HPZ7 | Leishmania braziliensis | 77% | 100% |
A4IDQ8 | Leishmania infantum | 92% | 100% |
E9ATR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |