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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AI06
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.415 |
CLV_PCSK_FUR_1 | 131 | 135 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.240 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.378 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.370 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.266 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.522 |
DOC_MAPK_gen_1 | 216 | 224 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 58 | 66 | PF00069 | 0.379 |
DOC_MAPK_HePTP_8 | 230 | 242 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 216 | 224 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.615 |
DOC_PP1_RVXF_1 | 227 | 233 | PF00149 | 0.561 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 112 | 121 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.523 |
LIG_Actin_RPEL_3 | 51 | 70 | PF02755 | 0.389 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 188 | 194 | PF00928 | 0.514 |
LIG_eIF4E_1 | 201 | 207 | PF01652 | 0.584 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.521 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.549 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.493 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.382 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.358 |
LIG_NRBOX | 37 | 43 | PF00104 | 0.431 |
LIG_Pex14_1 | 190 | 194 | PF04695 | 0.507 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.587 |
LIG_REV1ctd_RIR_1 | 240 | 248 | PF16727 | 0.562 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 201 | 204 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.418 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.517 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.595 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.339 |
LIG_SH3_4 | 260 | 267 | PF00018 | 0.602 |
LIG_TYR_ITSM | 167 | 174 | PF00017 | 0.483 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.629 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.654 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.503 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.655 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.692 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.652 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.519 |
MOD_LATS_1 | 52 | 58 | PF00433 | 0.431 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.533 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.616 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.424 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.424 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.527 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.329 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.430 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.442 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.430 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.553 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.609 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.416 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.592 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.364 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.482 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.528 |
TRG_NLS_MonoExtN_4 | 108 | 115 | PF00514 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 134 | 139 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFV7 | Leptomonas seymouri | 78% | 100% |
A0A0S4JY76 | Bodo saltans | 51% | 100% |
A0A1X0NLD5 | Trypanosomatidae | 70% | 100% |
A0A3Q8II78 | Leishmania donovani | 100% | 100% |
A4HQJ6 | Leishmania braziliensis | 90% | 100% |
D0A3P5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9AUA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q081 | Leishmania major | 95% | 100% |
V5BHN0 | Trypanosoma cruzi | 66% | 100% |