Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 24 |
NetGPI | no | yes: 0, no: 24 |
Related structures:
AlphaFold database: Q4Q6I6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.389 |
DOC_MAPK_gen_1 | 155 | 164 | PF00069 | 0.374 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.503 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.557 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.436 |
LIG_14-3-3_CanoR_1 | 285 | 290 | PF00244 | 0.689 |
LIG_Actin_WH2_2 | 88 | 105 | PF00022 | 0.544 |
LIG_ActinCP_CPI_1 | 278 | 295 | PF01115 | 0.493 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.569 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_2 | 55 | 61 | PF00533 | 0.323 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.474 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.538 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.534 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.483 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.462 |
LIG_LIR_Apic_2 | 6 | 10 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 172 | 182 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.306 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.436 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.449 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.669 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.441 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.547 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.391 |
LIG_UBA3_1 | 33 | 38 | PF00899 | 0.448 |
LIG_UBA3_1 | 75 | 79 | PF00899 | 0.289 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.396 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.511 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.346 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.483 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.660 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.509 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.535 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.374 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.431 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.312 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.473 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.520 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.392 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.513 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.516 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.462 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.471 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.507 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.727 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.448 |
MOD_N-GLC_2 | 262 | 264 | PF02516 | 0.472 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.488 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.504 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.626 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.544 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.498 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.508 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.545 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.684 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.489 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.396 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.359 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.536 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.537 |
MOD_SUMO_for_1 | 113 | 116 | PF00179 | 0.612 |
TRG_DiLeu_BaEn_1 | 86 | 91 | PF01217 | 0.283 |
TRG_DiLeu_BaEn_3 | 172 | 178 | PF01217 | 0.302 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.410 |
TRG_NLS_MonoExtN_4 | 122 | 128 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P348 | Leptomonas seymouri | 23% | 68% |
A0A0N0P4S1 | Leptomonas seymouri | 24% | 100% |
A0A1X0NK28 | Trypanosomatidae | 37% | 73% |
A0A3Q8IG21 | Leishmania donovani | 82% | 71% |
A0A3Q8IIE7 | Leishmania donovani | 78% | 95% |
A0A3S5H792 | Leishmania donovani | 25% | 100% |
A0A3S7WQB3 | Leishmania donovani | 22% | 71% |
A0A422NQZ1 | Trypanosoma rangeli | 33% | 72% |
A4H6C6 | Leishmania braziliensis | 24% | 76% |
A4HBK0 | Leishmania braziliensis | 23% | 100% |
A4HJ56 | Leishmania braziliensis | 69% | 68% |
A4HTM7 | Leishmania infantum | 22% | 71% |
A4HZL5 | Leishmania infantum | 25% | 100% |
A4I6H9 | Leishmania infantum | 83% | 71% |
E9AHL0 | Leishmania infantum | 79% | 95% |
E9AMG1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 71% |
E9AUW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B1M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9B1N5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9B1N6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 71% |
Q4Q6H8 | Leishmania major | 93% | 68% |
Q4QCL3 | Leishmania major | 27% | 100% |
Q4QI82 | Leishmania major | 23% | 74% |