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: A0A3Q8IAT2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.659 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.734 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.430 |
DEG_SCF_FBW7_1 | 148 | 154 | PF00400 | 0.521 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.536 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.525 |
DOC_CDC14_PxL_1 | 404 | 412 | PF14671 | 0.505 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.515 |
DOC_CKS1_1 | 517 | 522 | PF01111 | 0.783 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.527 |
DOC_CYCLIN_yCln2_LP_2 | 430 | 436 | PF00134 | 0.583 |
DOC_CYCLIN_yCln2_LP_2 | 456 | 462 | PF00134 | 0.557 |
DOC_MAPK_gen_1 | 142 | 148 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 398 | 407 | PF00069 | 0.687 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.778 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.489 |
DOC_PP4_MxPP_1 | 488 | 491 | PF00568 | 0.661 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.770 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 451 | 455 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.746 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.579 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.721 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.659 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.629 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.486 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.644 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.608 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.583 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.617 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.444 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.587 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.542 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.707 |
LIG_GBD_Chelix_1 | 177 | 185 | PF00786 | 0.325 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.487 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.525 |
LIG_MYND_3 | 134 | 138 | PF01753 | 0.531 |
LIG_NRBOX | 176 | 182 | PF00104 | 0.454 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.632 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.506 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.577 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.674 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 272 | 275 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.521 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.435 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.540 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.716 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.633 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.741 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.644 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.474 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.631 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.703 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.723 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.700 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.556 |
LIG_Sin3_3 | 442 | 449 | PF02671 | 0.760 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.602 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.485 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.642 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.587 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.511 |
LIG_UBA3_1 | 133 | 142 | PF00899 | 0.516 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.708 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.634 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.710 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.678 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.588 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.430 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.680 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.630 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.553 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.525 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.728 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.636 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.716 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.677 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.696 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.723 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.518 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.624 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.589 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.679 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.621 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.717 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.698 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.622 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.727 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.734 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.428 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.409 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.679 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.478 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.686 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.731 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.761 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.738 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.527 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.747 |
MOD_PKA_1 | 400 | 406 | PF00069 | 0.731 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.723 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.729 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.489 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.546 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.466 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.791 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.696 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 377 | 382 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 405 | 410 | PF01217 | 0.748 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.507 |
TRG_NLS_MonoExtN_4 | 254 | 261 | PF00514 | 0.514 |
TRG_NLS_MonoExtN_4 | 448 | 454 | PF00514 | 0.769 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT9 | Leptomonas seymouri | 58% | 93% |
A4HBP8 | Leishmania braziliensis | 83% | 100% |
A4HZ50 | Leishmania infantum | 100% | 100% |
D0A1Q2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AV18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QCG4 | Leishmania major | 90% | 100% |
V5BKP0 | Trypanosoma cruzi | 29% | 100% |