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: A0A3Q8IJS4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 269 | 273 | PF03568 | 0.428 |
CLV_Separin_Metazoa | 94 | 98 | PF03568 | 0.434 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.588 |
DOC_ANK_TNKS_1 | 133 | 140 | PF00023 | 0.559 |
DOC_CKS1_1 | 127 | 132 | PF01111 | 0.421 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 23 | 32 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.477 |
DOC_PP4_FxxP_1 | 24 | 27 | PF00568 | 0.500 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 66 | 74 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 83 | 99 | PF00022 | 0.450 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.456 |
LIG_EH1_1 | 237 | 245 | PF00400 | 0.402 |
LIG_EVH1_2 | 124 | 128 | PF00568 | 0.482 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.451 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.465 |
LIG_GBD_Chelix_1 | 176 | 184 | PF00786 | 0.409 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.464 |
LIG_PCNA_yPIPBox_3 | 199 | 212 | PF02747 | 0.398 |
LIG_Pex14_1 | 311 | 315 | PF04695 | 0.425 |
LIG_RPA_C_Fungi | 205 | 217 | PF08784 | 0.348 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.439 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.418 |
LIG_SH3_1 | 121 | 127 | PF00018 | 0.460 |
LIG_SH3_1 | 140 | 146 | PF00018 | 0.582 |
LIG_SH3_1 | 249 | 255 | PF00018 | 0.428 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.460 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.459 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.428 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.550 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.579 |
LIG_WW_1 | 366 | 369 | PF00397 | 0.652 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.587 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.439 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.392 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.548 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.668 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.435 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.469 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.468 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.528 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.434 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.680 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.509 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.599 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.440 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.581 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.601 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.456 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.599 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.423 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.537 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.505 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.390 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.420 |
MOD_PK_1 | 210 | 216 | PF00069 | 0.355 |
MOD_PK_1 | 25 | 31 | PF00069 | 0.543 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.427 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.381 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.642 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.476 |
MOD_PKB_1 | 23 | 31 | PF00069 | 0.539 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.580 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.549 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.576 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.454 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.538 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.526 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.439 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.418 |
MOD_SUMO_for_1 | 119 | 122 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 318 | 324 | PF00179 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2J5 | Leptomonas seymouri | 84% | 100% |
A0A0S4KDW2 | Bodo saltans | 53% | 100% |
A0A1X0P3G7 | Trypanosomatidae | 67% | 100% |
A0A3R7KL34 | Trypanosoma rangeli | 65% | 100% |
A4HQ45 | Leishmania braziliensis | 92% | 100% |
A4IC81 | Leishmania infantum | 99% | 100% |
D0A8R9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9ATW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q0N1 | Leishmania major | 97% | 100% |
V5BMB9 | Trypanosoma cruzi | 65% | 100% |