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: A0A3Q8IA19
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.498 |
CLV_PCSK_FUR_1 | 243 | 247 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 539 | 541 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.633 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.466 |
DEG_APCC_KENBOX_2 | 492 | 496 | PF00400 | 0.436 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.529 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.570 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.601 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.663 |
DEG_SPOP_SBC_1 | 529 | 533 | PF00917 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.562 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 32 | 42 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 403 | 409 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.445 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.570 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.600 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.551 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 217 | 226 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 231 | 241 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 294 | 299 | PF00244 | 0.455 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.551 |
LIG_Clathr_ClatBox_1 | 464 | 468 | PF01394 | 0.454 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.524 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.660 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.492 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.474 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.499 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.589 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.500 |
LIG_LIR_Gen_1 | 421 | 429 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.515 |
LIG_PCNA_yPIPBox_3 | 112 | 121 | PF02747 | 0.462 |
LIG_PCNA_yPIPBox_3 | 179 | 193 | PF02747 | 0.419 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.515 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.438 |
LIG_SH3_2 | 411 | 416 | PF14604 | 0.538 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.653 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 173 | 180 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 173 | 180 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 463 | 468 | PF11976 | 0.496 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.511 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.402 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.507 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.573 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.577 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.573 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.537 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.557 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.586 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.602 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.433 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.440 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.532 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.491 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.602 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.577 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.625 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.601 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.528 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.555 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.594 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.557 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.488 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.487 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.570 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.315 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.578 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.547 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.651 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.517 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.389 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.531 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.701 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.612 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.449 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.545 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.706 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.611 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.578 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.624 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.461 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.534 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.478 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.434 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.553 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.432 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.580 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.506 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.484 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.388 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.506 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.506 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.466 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.508 |
MOD_PKB_1 | 501 | 509 | PF00069 | 0.429 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.481 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.452 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.557 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.586 |
MOD_SUMO_for_1 | 298 | 301 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 124 | 134 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 133 | 138 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_4 | 173 | 179 | PF01217 | 0.539 |
TRG_DiLeu_LyEn_5 | 133 | 138 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.549 |
TRG_NLS_MonoExtC_3 | 498 | 503 | PF00514 | 0.423 |
TRG_NLS_MonoExtN_4 | 499 | 504 | PF00514 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 6 | 11 | PF00026 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I948 | Leptomonas seymouri | 44% | 87% |
A4H828 | Leishmania braziliensis | 70% | 100% |
A4HWF4 | Leishmania infantum | 100% | 100% |
E9AQ53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QFC9 | Leishmania major | 92% | 100% |