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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8S9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.489 |
CLV_Separin_Metazoa | 223 | 227 | PF03568 | 0.470 |
DEG_APCC_DBOX_1 | 46 | 54 | PF00400 | 0.479 |
DOC_MAPK_gen_1 | 147 | 154 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 117 | 125 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 147 | 154 | PF00069 | 0.477 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.601 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.457 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.607 |
LIG_Clathr_ClatBox_1 | 53 | 57 | PF01394 | 0.586 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.432 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.661 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.473 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.438 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.438 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.536 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.644 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.720 |
LIG_GBD_Chelix_1 | 160 | 168 | PF00786 | 0.608 |
LIG_Integrin_RGD_1 | 134 | 136 | PF01839 | 0.531 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 96 | 106 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.446 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.497 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.430 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.546 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.473 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.606 |
LIG_SH2_NCK_1 | 111 | 115 | PF00017 | 0.606 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 186 | 189 | PF00017 | 0.597 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.475 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.571 |
LIG_SUMO_SIM_anti_2 | 195 | 201 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 215 | 220 | PF11976 | 0.212 |
LIG_SUMO_SIM_anti_2 | 248 | 257 | PF11976 | 0.641 |
LIG_SUMO_SIM_anti_2 | 52 | 57 | PF11976 | 0.594 |
LIG_SUMO_SIM_par_1 | 229 | 236 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 248 | 257 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 52 | 57 | PF11976 | 0.594 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.469 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.455 |
LIG_TYR_ITSM | 107 | 114 | PF00017 | 0.610 |
LIG_UBA3_1 | 53 | 59 | PF00899 | 0.588 |
LIG_WRC_WIRS_1 | 102 | 107 | PF05994 | 0.451 |
MOD_CDK_SPxxK_3 | 93 | 100 | PF00069 | 0.476 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.251 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.479 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.552 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.654 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.588 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.440 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.599 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.552 |
MOD_Cter_Amidation | 145 | 148 | PF01082 | 0.554 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.546 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.472 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.380 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.502 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.593 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.591 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.607 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.434 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.620 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.555 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.491 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.598 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.499 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.399 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.557 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.408 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.447 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.459 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.446 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.548 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.551 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.559 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.476 |
MOD_SUMO_rev_2 | 52 | 61 | PF00179 | 0.373 |
TRG_DiLeu_BaEn_1 | 175 | 180 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_1 | 8 | 13 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7K2 | Leptomonas seymouri | 62% | 100% |
A0A3S7X096 | Leishmania donovani | 95% | 100% |
A4HFA6 | Leishmania braziliensis | 86% | 100% |
A4I2I3 | Leishmania infantum | 95% | 100% |
E9AYP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |