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: 3 |
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: Q4Q3F4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.658 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.486 |
DEG_SCF_FBW7_2 | 21 | 28 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 161 | 165 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 205 | 209 | PF00917 | 0.570 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.398 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.613 |
DOC_CYCLIN_RxL_1 | 304 | 314 | PF00134 | 0.452 |
DOC_CYCLIN_yCln2_LP_2 | 305 | 311 | PF00134 | 0.331 |
DOC_MAPK_DCC_7 | 479 | 487 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 479 | 487 | PF00069 | 0.504 |
DOC_PP1_RVXF_1 | 360 | 367 | PF00149 | 0.582 |
DOC_PP2B_LxvP_1 | 486 | 489 | PF13499 | 0.551 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.474 |
DOC_PP4_MxPP_1 | 459 | 462 | PF00568 | 0.587 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 411 | 415 | PF00244 | 0.567 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.497 |
LIG_EVH1_2 | 168 | 172 | PF00568 | 0.537 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.621 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.482 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.500 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.585 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.725 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.552 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.681 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.656 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.585 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.716 |
LIG_LIR_Apic_2 | 208 | 214 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 484 | 490 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 439 | 445 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 439 | 443 | PF02991 | 0.657 |
LIG_MAD2 | 39 | 47 | PF02301 | 0.603 |
LIG_PROFILIN_1 | 45 | 51 | PF00235 | 0.617 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.525 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.747 |
LIG_SH3_1 | 43 | 49 | PF00018 | 0.586 |
LIG_SH3_1 | 457 | 463 | PF00018 | 0.564 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.828 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.611 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.610 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.670 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.597 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.601 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.564 |
LIG_SH3_4 | 244 | 251 | PF00018 | 0.449 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.571 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.657 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.442 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.579 |
LIG_TRAF2_1 | 378 | 381 | PF00917 | 0.594 |
LIG_WW_1 | 462 | 465 | PF00397 | 0.601 |
MOD_CDK_SPK_2 | 21 | 26 | PF00069 | 0.672 |
MOD_CDK_SPK_2 | 299 | 304 | PF00069 | 0.397 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.550 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.629 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.593 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.614 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.607 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.645 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.572 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.574 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.512 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.497 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.585 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.607 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.818 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.587 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.721 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.648 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.609 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.473 |
MOD_GlcNHglycan | 27 | 31 | PF01048 | 0.636 |
MOD_GlcNHglycan | 446 | 450 | PF01048 | 0.577 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.748 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.545 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.587 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.612 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.686 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.570 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.672 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.634 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.628 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.496 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.688 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.518 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.459 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.490 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.637 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.560 |
MOD_PKB_1 | 9 | 17 | PF00069 | 0.567 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.480 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.577 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.605 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.736 |
MOD_Plk_2-3 | 339 | 345 | PF00069 | 0.604 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.587 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.494 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.708 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.660 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.699 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.703 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.611 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.463 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.467 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.476 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.456 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.665 |
MOD_SUMO_for_1 | 243 | 246 | PF00179 | 0.409 |
MOD_SUMO_for_1 | 25 | 28 | PF00179 | 0.691 |
MOD_SUMO_for_1 | 65 | 68 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 81 | 91 | PF00179 | 0.743 |
MOD_SUMO_rev_2 | 97 | 107 | PF00179 | 0.581 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_2 | 234 | 240 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P589 | Leptomonas seymouri | 30% | 68% |
A0A3Q8IGZ7 | Leishmania donovani | 86% | 100% |
A4H7D5 | Leishmania braziliensis | 52% | 71% |
A4I9M3 | Leishmania infantum | 87% | 100% |
E9B4M2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |