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: E9B684
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.711 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.767 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.766 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.813 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.762 |
CLV_PCSK_FUR_1 | 314 | 318 | PF00082 | 0.333 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.762 |
CLV_PCSK_PC7_1 | 446 | 452 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.778 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.523 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.699 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.587 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.736 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.723 |
DOC_USP7_MATH_2 | 395 | 401 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 461 | 465 | PF00244 | 0.741 |
LIG_BIR_III_2 | 245 | 249 | PF00653 | 0.625 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.594 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.571 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.561 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.611 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.726 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.439 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.610 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.630 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.615 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.787 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.748 |
LIG_Integrin_RGD_1 | 452 | 454 | PF01839 | 0.533 |
LIG_LIR_Apic_2 | 322 | 327 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.497 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.619 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 324 | 328 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.528 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.662 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.558 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.494 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.530 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.438 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.757 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.548 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.743 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.555 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.758 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.804 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.634 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.228 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.774 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.598 |
MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.369 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.744 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.380 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.698 |
MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.797 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.407 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.710 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.562 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.675 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.808 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.570 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.579 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.526 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.744 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.694 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.689 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.661 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.462 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.638 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.379 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.456 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.530 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.438 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.545 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.602 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.721 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.755 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.391 |
MOD_NEK2_2 | 345 | 350 | PF00069 | 0.506 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.694 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.590 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.357 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.794 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.714 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.793 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.785 |
MOD_PKB_1 | 450 | 458 | PF00069 | 0.529 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.486 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.438 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.415 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.528 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.774 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.389 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.632 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.691 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.731 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.713 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.519 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.391 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.696 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.580 |
MOD_SUMO_rev_2 | 50 | 58 | PF00179 | 0.691 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.809 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.794 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.774 |
TRG_NES_CRM1_1 | 381 | 391 | PF08389 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT1 | Leptomonas seymouri | 53% | 100% |
A0A0S4JH24 | Bodo saltans | 36% | 100% |
A0A3Q8IJ10 | Leishmania donovani | 89% | 100% |
A0A422NNS8 | Trypanosoma rangeli | 43% | 100% |
A4HMM6 | Leishmania braziliensis | 70% | 99% |
A4IBA4 | Leishmania infantum | 89% | 100% |
E9AF28 | Leishmania major | 86% | 100% |