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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B5G7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 443 | 447 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.734 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.839 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.839 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.786 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.673 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.598 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.764 |
DOC_CYCLIN_yCln2_LP_2 | 432 | 438 | PF00134 | 0.748 |
DOC_MAPK_JIP1_4 | 345 | 351 | PF00069 | 0.728 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.510 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.729 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.540 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.719 |
DOC_USP7_UBL2_3 | 527 | 531 | PF12436 | 0.556 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.769 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 5 | 14 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 516 | 520 | PF00244 | 0.613 |
LIG_AP2alpha_2 | 167 | 169 | PF02296 | 0.393 |
LIG_APCC_Cbox_2 | 15 | 21 | PF00515 | 0.483 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.488 |
LIG_CtBP_PxDLS_1 | 493 | 497 | PF00389 | 0.350 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.813 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.565 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.603 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.716 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.751 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.521 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.645 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.590 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.437 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.600 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 301 | 305 | PF00017 | 0.445 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.592 |
LIG_SH2_SRC | 301 | 304 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.492 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.807 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.599 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.709 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.581 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.772 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.767 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.657 |
LIG_TRAF2_2 | 438 | 443 | PF00917 | 0.648 |
LIG_TYR_ITSM | 200 | 207 | PF00017 | 0.355 |
MOD_CDC14_SPxK_1 | 29 | 32 | PF00782 | 0.574 |
MOD_CDK_SPK_2 | 332 | 337 | PF00069 | 0.732 |
MOD_CDK_SPK_2 | 466 | 471 | PF00069 | 0.608 |
MOD_CDK_SPxK_1 | 26 | 32 | PF00069 | 0.584 |
MOD_CDK_SPxxK_3 | 332 | 339 | PF00069 | 0.734 |
MOD_CDK_SPxxK_3 | 60 | 67 | PF00069 | 0.767 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.667 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.784 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.680 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.622 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.555 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.742 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.683 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.602 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.520 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.624 |
MOD_DYRK1A_RPxSP_1 | 26 | 30 | PF00069 | 0.585 |
MOD_DYRK1A_RPxSP_1 | 60 | 64 | PF00069 | 0.771 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.737 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.594 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.743 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.686 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.586 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.571 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.748 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.640 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.642 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.579 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.775 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.574 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.539 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.486 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.655 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.586 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.608 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.760 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.642 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.759 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.696 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.586 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.531 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.823 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.617 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.489 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.504 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.517 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.537 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.811 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.735 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.374 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.632 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.644 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.679 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.564 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.586 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.621 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.820 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.576 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.492 |
MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.617 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.689 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.523 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.729 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.539 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.733 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.801 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.612 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.646 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.766 |
MOD_SUMO_for_1 | 239 | 242 | PF00179 | 0.571 |
MOD_SUMO_for_1 | 438 | 441 | PF00179 | 0.767 |
MOD_SUMO_rev_2 | 242 | 251 | PF00179 | 0.653 |
MOD_SUMO_rev_2 | 83 | 91 | PF00179 | 0.621 |
TRG_DiLeu_BaEn_2 | 164 | 170 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_4 | 151 | 157 | PF01217 | 0.811 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.441 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.657 |
TRG_NLS_MonoCore_2 | 382 | 387 | PF00514 | 0.838 |
TRG_NLS_MonoExtC_3 | 382 | 387 | PF00514 | 0.838 |
TRG_NLS_MonoExtC_3 | 421 | 426 | PF00514 | 0.734 |
TRG_NLS_MonoExtN_4 | 383 | 389 | PF00514 | 0.812 |
TRG_NLS_MonoExtN_4 | 419 | 426 | PF00514 | 0.727 |
TRG_Pf-PMV_PEXEL_1 | 26 | 31 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8INS4 | Leishmania donovani | 79% | 100% |
A4HB95 | Leishmania braziliensis | 60% | 100% |
A4IAE3 | Leishmania infantum | 79% | 100% |
Q4Q2G8 | Leishmania major | 78% | 100% |