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: A0A3Q8IHY9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.548 |
CLV_MEL_PAP_1 | 451 | 457 | PF00089 | 0.623 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.684 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.642 |
CLV_Separin_Metazoa | 75 | 79 | PF03568 | 0.527 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.603 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.567 |
DOC_CDC14_PxL_1 | 126 | 134 | PF14671 | 0.519 |
DOC_CKS1_1 | 440 | 445 | PF01111 | 0.602 |
DOC_CYCLIN_RxL_1 | 113 | 123 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 416 | 422 | PF00134 | 0.576 |
DOC_PP2B_LxvP_1 | 70 | 73 | PF13499 | 0.615 |
DOC_PP4_MxPP_1 | 404 | 407 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.616 |
DOC_USP7_MATH_2 | 136 | 142 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 216 | 224 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 396 | 402 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 446 | 450 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.606 |
LIG_Actin_WH2_2 | 197 | 214 | PF00022 | 0.520 |
LIG_BIR_III_4 | 360 | 364 | PF00653 | 0.535 |
LIG_CtBP_PxDLS_1 | 73 | 77 | PF00389 | 0.556 |
LIG_EVH1_2 | 406 | 410 | PF00568 | 0.652 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.622 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.533 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.703 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.614 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.642 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.493 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.651 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.493 |
LIG_GBD_Chelix_1 | 118 | 126 | PF00786 | 0.573 |
LIG_LIR_Gen_1 | 178 | 185 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 497 | 501 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 17 | 21 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 497 | 501 | PF02991 | 0.701 |
LIG_MYND_3 | 129 | 133 | PF01753 | 0.529 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.503 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 206 | 213 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 96 | 101 | PF11976 | 0.534 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.551 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.522 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.563 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 245 | 252 | PF00069 | 0.563 |
MOD_CDK_SPxxK_3 | 439 | 446 | PF00069 | 0.622 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.566 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.709 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.794 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.651 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.679 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.588 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.678 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.654 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.624 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.545 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.493 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.630 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.504 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.655 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.535 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.502 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.705 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.645 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.532 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.637 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.609 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.638 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.597 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.653 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.569 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.662 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.595 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.662 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.609 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.625 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.529 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.631 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.600 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.597 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.588 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.596 |
MOD_LATS_1 | 452 | 458 | PF00433 | 0.608 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.498 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.629 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.665 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.654 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.405 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.587 |
MOD_NEK2_2 | 238 | 243 | PF00069 | 0.588 |
MOD_OFUCOSY | 253 | 258 | PF10250 | 0.569 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.585 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.528 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.481 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.684 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.683 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.630 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.649 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.590 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.588 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.604 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.613 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.609 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.674 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.511 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.478 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.631 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.594 |
MOD_Plk_2-3 | 312 | 318 | PF00069 | 0.602 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.647 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.559 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.647 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.633 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.598 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.682 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.611 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.590 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.573 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.623 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.615 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.541 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_1 | 206 | 211 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7S4 | Leptomonas seymouri | 43% | 95% |
A4HG99 | Leishmania braziliensis | 70% | 100% |
A4I3D3 | Leishmania infantum | 99% | 100% |
E9AZM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q8L1 | Leishmania major | 90% | 100% |