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 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AVC6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.533 |
CLV_PCSK_FUR_1 | 253 | 257 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.533 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.555 |
DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 89 | 93 | PF00917 | 0.595 |
DOC_AGCK_PIF_1 | 45 | 50 | PF00069 | 0.566 |
DOC_CYCLIN_RxL_1 | 15 | 24 | PF00134 | 0.553 |
DOC_PP1_RVXF_1 | 65 | 71 | PF00149 | 0.598 |
DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.551 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.664 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.652 |
LIG_14-3-3_CanoR_1 | 260 | 267 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.610 |
LIG_APCC_ABBA_1 | 115 | 120 | PF00400 | 0.528 |
LIG_APCC_ABBA_1 | 194 | 199 | PF00400 | 0.612 |
LIG_APCC_ABBAyCdc20_2 | 193 | 199 | PF00400 | 0.603 |
LIG_CaM_IQ_9 | 27 | 42 | PF13499 | 0.548 |
LIG_Clathr_ClatBox_1 | 116 | 120 | PF01394 | 0.508 |
LIG_Clathr_ClatBox_1 | 20 | 24 | PF01394 | 0.478 |
LIG_CtBP_PxDLS_1 | 111 | 115 | PF00389 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 254 | 259 | PF00928 | 0.620 |
LIG_DLG_GKlike_1 | 40 | 47 | PF00625 | 0.487 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.452 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.465 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.511 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.574 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.517 |
LIG_Pex14_1 | 222 | 226 | PF04695 | 0.570 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.557 |
LIG_PTB_Apo_2 | 217 | 224 | PF02174 | 0.486 |
LIG_REV1ctd_RIR_1 | 83 | 92 | PF16727 | 0.631 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.468 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.620 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.544 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.632 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.598 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.608 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.518 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.503 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.557 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.674 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.669 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.666 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.490 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.643 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.537 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.568 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.669 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.628 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.530 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.514 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.293 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.506 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.623 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.577 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.523 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.518 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.594 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.616 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.572 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.528 |
MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.636 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.491 |
MOD_SUMO_rev_2 | 141 | 151 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 112 | 117 | PF01217 | 0.586 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3V9 | Leptomonas seymouri | 62% | 98% |
A0A0S4IH77 | Bodo saltans | 29% | 100% |
A0A1X0NHE8 | Trypanosomatidae | 42% | 100% |
A0A3S7WWT7 | Leishmania donovani | 90% | 100% |
A4HBY9 | Leishmania braziliensis | 80% | 100% |
A4HZD9 | Leishmania infantum | 91% | 100% |
D0A146 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4QC53 | Leishmania major | 92% | 100% |
V5B1U8 | Trypanosoma cruzi | 38% | 100% |