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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H4A8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.610 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.523 |
CLV_Separin_Metazoa | 168 | 172 | PF03568 | 0.595 |
DOC_CYCLIN_RxL_1 | 157 | 164 | PF00134 | 0.544 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.506 |
DOC_MAPK_DCC_7 | 308 | 317 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 57 | 65 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 308 | 317 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 353 | 361 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 358 | 364 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.567 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.680 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 224 | 231 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.448 |
LIG_deltaCOP1_diTrp_1 | 177 | 183 | PF00928 | 0.431 |
LIG_deltaCOP1_diTrp_1 | 230 | 235 | PF00928 | 0.561 |
LIG_deltaCOP1_diTrp_1 | 354 | 363 | PF00928 | 0.427 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.737 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.440 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.472 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.457 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.537 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.586 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.571 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.512 |
LIG_HCF-1_HBM_1 | 125 | 128 | PF13415 | 0.326 |
LIG_Integrin_RGD_1 | 171 | 173 | PF01839 | 0.629 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 297 | 306 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.588 |
LIG_PALB2_WD40_1 | 146 | 154 | PF16756 | 0.451 |
LIG_Pex14_1 | 179 | 183 | PF04695 | 0.439 |
LIG_Pex14_1 | 231 | 235 | PF04695 | 0.563 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 128 | 131 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.502 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.308 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.499 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.447 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.622 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.561 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.477 |
LIG_UBA3_1 | 262 | 266 | PF00899 | 0.410 |
LIG_UBA3_1 | 303 | 310 | PF00899 | 0.451 |
LIG_WW_3 | 157 | 161 | PF00397 | 0.423 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.347 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.477 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.640 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.684 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.619 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.661 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.565 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.573 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.574 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.520 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.768 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.415 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.741 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.661 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.670 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.713 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.636 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.514 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.588 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.534 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.714 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.778 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.497 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.585 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.445 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.621 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.496 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.486 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.439 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.601 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.516 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.570 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.570 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.507 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.686 |
MOD_PKB_1 | 222 | 230 | PF00069 | 0.572 |
MOD_PKB_1 | 238 | 246 | PF00069 | 0.580 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.456 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.482 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.487 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.600 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.432 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.476 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 212 | 215 | PF00179 | 0.657 |
MOD_SUMO_for_1 | 255 | 258 | PF00179 | 0.499 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.577 |
MOD_SUMO_rev_2 | 195 | 205 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 215 | 223 | PF00179 | 0.380 |
TRG_DiLeu_BaEn_3 | 111 | 117 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_4 | 354 | 360 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.607 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.573 |
TRG_NES_CRM1_1 | 358 | 372 | PF08389 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT4 | Leptomonas seymouri | 82% | 100% |
A0A0S4IKX2 | Bodo saltans | 60% | 100% |
A0A1X0NJW6 | Trypanosomatidae | 64% | 99% |
A0A3S5H5I6 | Leishmania donovani | 90% | 100% |
A0A422ND56 | Trypanosoma rangeli | 62% | 100% |
A4HSH9 | Leishmania infantum | 91% | 100% |
C9ZUC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AKG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QJE5 | Leishmania major | 89% | 100% |
V5AVB4 | Trypanosoma cruzi | 66% | 100% |