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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B0A6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.758 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.473 |
CLV_PCSK_FUR_1 | 275 | 279 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.672 |
CLV_PCSK_PC7_1 | 476 | 482 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.576 |
DEG_SPOP_SBC_1 | 131 | 135 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 223 | 227 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.533 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.687 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.434 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.583 |
DOC_ANK_TNKS_1 | 337 | 344 | PF00023 | 0.503 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.516 |
DOC_MAPK_gen_1 | 362 | 373 | PF00069 | 0.700 |
DOC_MAPK_MEF2A_6 | 417 | 425 | PF00069 | 0.614 |
DOC_MAPK_MEF2A_6 | 484 | 492 | PF00069 | 0.642 |
DOC_MAPK_RevD_3 | 143 | 157 | PF00069 | 0.401 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 156 | 166 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 315 | 319 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 92 | 98 | PF00244 | 0.543 |
LIG_Actin_WH2_2 | 107 | 125 | PF00022 | 0.536 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.650 |
LIG_Clathr_ClatBox_1 | 59 | 63 | PF01394 | 0.618 |
LIG_deltaCOP1_diTrp_1 | 482 | 492 | PF00928 | 0.637 |
LIG_eIF4E_1 | 440 | 446 | PF01652 | 0.649 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.395 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.518 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.603 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.710 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.462 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.472 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.707 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.747 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.638 |
LIG_Integrin_RGD_1 | 366 | 368 | PF01839 | 0.678 |
LIG_LIR_Apic_2 | 437 | 443 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.549 |
LIG_MYND_1 | 443 | 447 | PF01753 | 0.641 |
LIG_PDZ_Class_2 | 487 | 492 | PF00595 | 0.646 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.648 |
LIG_SH2_PTP2 | 449 | 452 | PF00017 | 0.627 |
LIG_SH2_SRC | 444 | 447 | PF00017 | 0.612 |
LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.648 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.800 |
LIG_SUMO_SIM_anti_2 | 400 | 405 | PF11976 | 0.695 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 402 | 408 | PF11976 | 0.720 |
LIG_TYR_ITIM | 153 | 158 | PF00017 | 0.407 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.734 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.619 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.568 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.600 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.705 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.666 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.564 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.562 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.638 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.532 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.466 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.529 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.378 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.650 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.724 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.679 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.450 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.432 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.607 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.595 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.594 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.694 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.649 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.732 |
MOD_GlcNHglycan | 393 | 397 | PF01048 | 0.644 |
MOD_GlcNHglycan | 436 | 440 | PF01048 | 0.718 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.776 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.755 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.679 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.648 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.377 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.516 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.698 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.666 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.628 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.651 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.507 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.628 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.586 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.473 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.335 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.618 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.678 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.617 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.516 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.510 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.491 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.586 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.696 |
MOD_PK_1 | 417 | 423 | PF00069 | 0.497 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.512 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.465 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.560 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.634 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.683 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.602 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.339 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.337 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.718 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.632 |
MOD_Plk_2-3 | 430 | 436 | PF00069 | 0.592 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.680 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.674 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.501 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.674 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.667 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.705 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.549 |
TRG_DiLeu_BaEn_1 | 441 | 446 | PF01217 | 0.646 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.601 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.500 |
TRG_NLS_MonoExtC_3 | 361 | 366 | PF00514 | 0.693 |
TRG_NLS_MonoExtN_4 | 360 | 367 | PF00514 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYA9 | Leptomonas seymouri | 50% | 100% |
A0A1X0NQL1 | Trypanosomatidae | 28% | 100% |
A0A3Q8IE22 | Leishmania donovani | 86% | 100% |
A0A3R7JYS6 | Trypanosoma rangeli | 27% | 100% |
A4HGY7 | Leishmania braziliensis | 73% | 100% |
A4I419 | Leishmania infantum | 82% | 100% |
Q4Q7X8 | Leishmania major | 87% | 100% |