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: E9B4Q8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.687 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.658 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.667 |
DOC_ANK_TNKS_1 | 298 | 305 | PF00023 | 0.645 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.741 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.672 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 437 | 446 | PF00069 | 0.685 |
DOC_MAPK_JIP1_4 | 77 | 83 | PF00069 | 0.545 |
DOC_PP1_RVXF_1 | 114 | 120 | PF00149 | 0.502 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.308 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.698 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.501 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.717 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 352 | 361 | PF00244 | 0.752 |
LIG_Actin_WH2_2 | 538 | 554 | PF00022 | 0.772 |
LIG_BIR_III_4 | 236 | 240 | PF00653 | 0.746 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 393 | 399 | PF00928 | 0.507 |
LIG_deltaCOP1_diTrp_1 | 411 | 415 | PF00928 | 0.578 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.547 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.558 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.819 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.692 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.829 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.756 |
LIG_LIR_Apic_2 | 108 | 114 | PF02991 | 0.484 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.780 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.558 |
LIG_LIR_Apic_2 | 369 | 374 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 5 | 15 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.478 |
LIG_PCNA_yPIPBox_3 | 417 | 431 | PF02747 | 0.570 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.692 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.684 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.778 |
LIG_SH2_NCK_1 | 371 | 375 | PF00017 | 0.633 |
LIG_SH2_SRC | 427 | 430 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.683 |
LIG_SH3_1 | 433 | 439 | PF00018 | 0.595 |
LIG_SH3_2 | 436 | 441 | PF14604 | 0.644 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.788 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.615 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.640 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.595 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.723 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.575 |
LIG_UBA3_1 | 544 | 552 | PF00899 | 0.643 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.508 |
LIG_WW_3 | 379 | 383 | PF00397 | 0.693 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.654 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.568 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.698 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.561 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.788 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.798 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.756 |
MOD_CMANNOS | 396 | 399 | PF00535 | 0.507 |
MOD_CMANNOS | 412 | 415 | PF00535 | 0.587 |
MOD_Cter_Amidation | 239 | 242 | PF01082 | 0.697 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.685 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.683 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.702 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.661 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.523 |
MOD_GlcNHglycan | 451 | 455 | PF01048 | 0.696 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.593 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.686 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.640 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.732 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.635 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.744 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.761 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.534 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.509 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.466 |
MOD_NEK2_2 | 359 | 364 | PF00069 | 0.682 |
MOD_OFUCOSY | 272 | 278 | PF10250 | 0.522 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.511 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.747 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.470 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.668 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.535 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.503 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.539 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.533 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.509 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.780 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.654 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.776 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.588 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.548 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.742 |
TRG_DiLeu_BaLyEn_6 | 361 | 366 | PF01217 | 0.529 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.509 |
TRG_NLS_MonoCore_2 | 439 | 444 | PF00514 | 0.472 |
TRG_NLS_MonoExtC_3 | 439 | 445 | PF00514 | 0.669 |
TRG_NLS_MonoExtN_4 | 437 | 444 | PF00514 | 0.660 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A7 | Leptomonas seymouri | 52% | 100% |
A0A3S7X7L7 | Leishmania donovani | 88% | 100% |
A4HAK0 | Leishmania braziliensis | 74% | 99% |
A4I9P4 | Leishmania infantum | 88% | 100% |
Q4Q3B8 | Leishmania major | 91% | 99% |