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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AX38
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 237 | 243 | PF00089 | 0.298 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.552 |
CLV_PCSK_FUR_1 | 508 | 512 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.556 |
CLV_PCSK_PC7_1 | 277 | 283 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 506 | 512 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.585 |
CLV_Separin_Metazoa | 472 | 476 | PF03568 | 0.584 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.435 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.798 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.574 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.689 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.786 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.542 |
DOC_MAPK_MEF2A_6 | 334 | 341 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 334 | 342 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 441 | 447 | PF00149 | 0.601 |
DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.533 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.559 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.718 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 364 | 374 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 508 | 516 | PF00244 | 0.615 |
LIG_Actin_WH2_2 | 134 | 151 | PF00022 | 0.644 |
LIG_Actin_WH2_2 | 203 | 219 | PF00022 | 0.470 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.534 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.748 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.651 |
LIG_Clathr_ClatBox_1 | 347 | 351 | PF01394 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 340 | 350 | PF00928 | 0.504 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.607 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.584 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.334 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.785 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.684 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.702 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.602 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.596 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.570 |
LIG_LIR_Apic_2 | 340 | 345 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.480 |
LIG_SH2_SRC | 470 | 473 | PF00017 | 0.558 |
LIG_SH2_SRC | 496 | 499 | PF00017 | 0.609 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.553 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.780 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.715 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.658 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.707 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 35 | 42 | PF11976 | 0.730 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.675 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.761 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.723 |
LIG_UBA3_1 | 480 | 485 | PF00899 | 0.559 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.755 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.790 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.531 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.692 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.682 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.606 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.745 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.760 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.443 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.805 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.652 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.673 |
MOD_GlcNHglycan | 20 | 24 | PF01048 | 0.705 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.753 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.644 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.612 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.672 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.763 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.713 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.549 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.634 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.595 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.515 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.433 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.603 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.573 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.699 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.792 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.749 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.573 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.649 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.609 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.596 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.482 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.732 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.356 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.669 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.723 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.582 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.431 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.457 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.585 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.739 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.625 |
MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.721 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.621 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.565 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.771 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.687 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.651 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.709 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.692 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.760 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.609 |
MOD_SUMO_for_1 | 484 | 487 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_2 | 441 | 447 | PF01217 | 0.601 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P7 | Leptomonas seymouri | 57% | 95% |
A0A0S4J1F8 | Bodo saltans | 26% | 95% |
A0A1X0NW49 | Trypanosomatidae | 34% | 100% |
A0A3Q8IMW3 | Leishmania donovani | 93% | 100% |
A0A422NWS4 | Trypanosoma rangeli | 34% | 100% |
A4HDQ4 | Leishmania braziliensis | 85% | 100% |
A4I100 | Leishmania infantum | 93% | 100% |
C9ZWA9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QAD8 | Leishmania major | 92% | 100% |