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: A4HRK2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.822 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.817 |
CLV_PCSK_PC1ET2_1 | 484 | 486 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.590 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.667 |
DEG_SCF_FBW7_1 | 201 | 206 | PF00400 | 0.620 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.712 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.578 |
DOC_MAPK_gen_1 | 277 | 286 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 386 | 393 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 484 | 491 | PF00069 | 0.588 |
DOC_PP1_RVXF_1 | 488 | 494 | PF00149 | 0.574 |
DOC_PP4_MxPP_1 | 235 | 238 | PF00568 | 0.597 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.694 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 130 | 140 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 424 | 434 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 455 | 462 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 512 | 517 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.682 |
LIG_BIR_III_4 | 364 | 368 | PF00653 | 0.652 |
LIG_BIR_III_4 | 394 | 398 | PF00653 | 0.663 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.635 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.669 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.567 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.589 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.664 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 163 | 169 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 467 | 471 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 170 | 174 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.666 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.638 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.636 |
LIG_SH2_GRB2like | 447 | 450 | PF00017 | 0.668 |
LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.573 |
LIG_SH2_SRC | 468 | 471 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.558 |
LIG_SH3_1 | 299 | 305 | PF00018 | 0.698 |
LIG_SH3_2 | 239 | 244 | PF14604 | 0.614 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.649 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.722 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.692 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.663 |
MOD_CDC14_SPxK_1 | 241 | 244 | PF00782 | 0.615 |
MOD_CDK_SPxK_1 | 238 | 244 | PF00069 | 0.613 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.744 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.733 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.529 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.836 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.720 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.714 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.655 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.554 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.618 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.705 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.678 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.668 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.863 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.724 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.789 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.694 |
MOD_GlcNHglycan | 256 | 260 | PF01048 | 0.641 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.737 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.805 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.839 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.657 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.755 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.794 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.738 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.658 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.815 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.679 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.846 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.800 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.588 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.647 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.564 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.633 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.596 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.737 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.645 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.722 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.680 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.636 |
MOD_OFUCOSY | 453 | 459 | PF10250 | 0.674 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.680 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.706 |
MOD_PKA_1 | 345 | 351 | PF00069 | 0.745 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.639 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.559 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.669 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.734 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.770 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.712 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.602 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.727 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.609 |
MOD_PKB_1 | 39 | 47 | PF00069 | 0.627 |
MOD_PKB_1 | 510 | 518 | PF00069 | 0.601 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.668 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.466 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.599 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.670 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.525 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.631 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.583 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.648 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.695 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.738 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.746 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.726 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.718 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.710 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_1 | 487 | 492 | PF01217 | 0.574 |
TRG_DiLeu_LyEn_5 | 487 | 492 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.805 |
TRG_ER_diArg_1 | 476 | 478 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 509 | 512 | PF00400 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A451EJD3 | Leishmania donovani | 99% | 100% |
A4H394 | Leishmania braziliensis | 61% | 100% |
E9AC70 | Leishmania major | 89% | 100% |
E9AJG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 96% |