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: A0A3S7WR07
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 496 | 500 | PF00656 | 0.651 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.339 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.751 |
DEG_APCC_DBOX_1 | 52 | 60 | PF00400 | 0.510 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.731 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.710 |
DOC_CYCLIN_RxL_1 | 466 | 476 | PF00134 | 0.648 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.672 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 121 | 125 | PF12436 | 0.552 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 329 | 336 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 362 | 370 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 442 | 448 | PF00244 | 0.713 |
LIG_AP2alpha_2 | 388 | 390 | PF02296 | 0.703 |
LIG_BIR_III_4 | 499 | 503 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.699 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.562 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.591 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.731 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.697 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.721 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.611 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.327 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.587 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.745 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.542 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.700 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.673 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.517 |
LIG_GBD_Chelix_1 | 134 | 142 | PF00786 | 0.531 |
LIG_GBD_Chelix_1 | 77 | 85 | PF00786 | 0.495 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.641 |
LIG_PCNA_yPIPBox_3 | 72 | 81 | PF02747 | 0.562 |
LIG_RPA_C_Fungi | 79 | 91 | PF08784 | 0.539 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.655 |
LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.576 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.701 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.734 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.630 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.785 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.525 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.563 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.613 |
LIG_UBA3_1 | 81 | 89 | PF00899 | 0.518 |
LIG_WW_1 | 14 | 17 | PF00397 | 0.686 |
MOD_CDK_SPxxK_3 | 347 | 354 | PF00069 | 0.704 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.510 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.598 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.713 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.573 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.549 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.626 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.752 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.556 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.776 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.753 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.638 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.758 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.588 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.627 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.736 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.558 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.681 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.666 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.719 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.707 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.736 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.665 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.653 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.654 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.683 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.747 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.743 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.673 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.670 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.688 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.714 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.614 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.719 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.796 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.601 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.666 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.620 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.631 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.655 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.660 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.633 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.796 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.760 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.718 |
MOD_LATS_1 | 220 | 226 | PF00433 | 0.719 |
MOD_LATS_1 | 410 | 416 | PF00433 | 0.664 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.595 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.546 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.654 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.615 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.740 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.482 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.697 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.475 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.557 |
MOD_NEK2_2 | 258 | 263 | PF00069 | 0.548 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.559 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.570 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.649 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.661 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.665 |
MOD_PK_1 | 73 | 79 | PF00069 | 0.528 |
MOD_PKA_1 | 90 | 96 | PF00069 | 0.441 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.562 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.717 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.713 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.533 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.441 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.827 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.501 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.749 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.485 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.651 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.688 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.466 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.805 |
MOD_SUMO_for_1 | 127 | 130 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 105 | 113 | PF00179 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 466 | 471 | PF01217 | 0.693 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.559 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.483 |
TRG_NLS_Bipartite_1 | 72 | 93 | PF00514 | 0.547 |
TRG_NLS_MonoCore_2 | 88 | 93 | PF00514 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 250 | 254 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 282 | 287 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6X5 | Leptomonas seymouri | 55% | 67% |
A0A0S4JC19 | Bodo saltans | 27% | 100% |
A0A3R7MLU6 | Trypanosoma rangeli | 30% | 100% |
A4H5Z7 | Leishmania braziliensis | 77% | 100% |
A4HUC3 | Leishmania infantum | 99% | 100% |
E9AN22 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QHK4 | Leishmania major | 92% | 100% |