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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q5A4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 434 | 438 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.587 |
CLV_PCSK_FUR_1 | 349 | 353 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 347 | 353 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.714 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.692 |
DEG_APCC_KENBOX_2 | 180 | 184 | PF00400 | 0.553 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.639 |
DEG_SPOP_SBC_1 | 428 | 432 | PF00917 | 0.703 |
DOC_ANK_TNKS_1 | 332 | 339 | PF00023 | 0.542 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.683 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.659 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 429 | 436 | PF00244 | 0.724 |
LIG_Actin_WH2_2 | 453 | 469 | PF00022 | 0.557 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.619 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.726 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.601 |
LIG_EH1_1 | 30 | 38 | PF00400 | 0.678 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.610 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.647 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.655 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.771 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.798 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.722 |
LIG_LIR_Gen_1 | 150 | 157 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 294 | 305 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 462 | 473 | PF02991 | 0.702 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.545 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.614 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.636 |
LIG_REV1ctd_RIR_1 | 58 | 66 | PF16727 | 0.587 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.686 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.711 |
LIG_SH3_1 | 26 | 32 | PF00018 | 0.640 |
LIG_SH3_2 | 29 | 34 | PF14604 | 0.663 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.663 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.572 |
LIG_Sin3_3 | 109 | 116 | PF02671 | 0.639 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.647 |
LIG_TRAF2_1 | 403 | 406 | PF00917 | 0.787 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.588 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.482 |
LIG_UBA3_1 | 126 | 132 | PF00899 | 0.568 |
MOD_CDK_SPK_2 | 424 | 429 | PF00069 | 0.629 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.652 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.622 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.742 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.708 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.839 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.765 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.620 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.762 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.600 |
MOD_GlcNHglycan | 386 | 390 | PF01048 | 0.733 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.627 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.627 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.539 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.702 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.693 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.590 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.820 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.710 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.708 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.586 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.716 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.738 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.683 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.426 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.670 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.644 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.556 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.831 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.726 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.385 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.644 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.692 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.690 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.630 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.775 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.660 |
TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.618 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.614 |
TRG_DiLeu_BaEn_4 | 168 | 174 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.640 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.710 |
TRG_NES_CRM1_1 | 124 | 140 | PF08389 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMW1 | Leptomonas seymouri | 40% | 85% |
A0A3Q8IG72 | Leishmania donovani | 85% | 100% |
A0A3R7MFC1 | Trypanosoma rangeli | 28% | 82% |
A4HKG3 | Leishmania braziliensis | 59% | 95% |
A4I7Z1 | Leishmania infantum | 86% | 100% |
E9B2V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |