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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QDM5
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 5 |
GO:0005509 | calcium ion binding | 5 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 182 | 186 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.478 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.515 |
CLV_PCSK_PC7_1 | 81 | 87 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.517 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.284 |
DEG_SCF_FBW7_2 | 122 | 129 | PF00400 | 0.595 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.577 |
DOC_PP1_RVXF_1 | 129 | 136 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 31 | 38 | PF00149 | 0.419 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 106 | 110 | PF12436 | 0.602 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.426 |
LIG_CaM_NSCaTE_8 | 209 | 216 | PF13499 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 134 | 138 | PF00928 | 0.336 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.418 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.426 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.507 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.489 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.614 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.472 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.470 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.483 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.661 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.416 |
LIG_LIR_Apic_2 | 214 | 220 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 134 | 139 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.381 |
LIG_PDZ_Class_3 | 251 | 256 | PF00595 | 0.578 |
LIG_Rb_LxCxE_1 | 134 | 153 | PF01857 | 0.352 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 217 | 220 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.504 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.682 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.442 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.581 |
LIG_SUMO_SIM_par_1 | 120 | 125 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 174 | 182 | PF11976 | 0.541 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.481 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.496 |
LIG_UBA3_1 | 24 | 33 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 34 | 39 | PF05994 | 0.398 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.431 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.591 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.490 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.380 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.604 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.688 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.595 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.507 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.456 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.452 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.582 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.519 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.569 |
MOD_PKA_1 | 110 | 116 | PF00069 | 0.695 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.617 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.424 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.606 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.586 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.442 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.562 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.611 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.463 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.443 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.399 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.452 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.597 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 79 | 82 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 123 | 133 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_1 | 192 | 197 | PF01217 | 0.545 |
TRG_DiLeu_BaEn_4 | 152 | 158 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.413 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBL1 | Leptomonas seymouri | 75% | 100% |
A0A0S4IRK8 | Bodo saltans | 48% | 84% |
A0A1X0P7F4 | Trypanosomatidae | 61% | 98% |
A0A3S7WVC9 | Leishmania donovani | 96% | 100% |
A0A422NPY0 | Trypanosoma rangeli | 57% | 99% |
A4H9R5 | Leishmania braziliensis | 85% | 100% |
A4HY34 | Leishmania infantum | 96% | 100% |
D0A550 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 70% |
E9ARU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D4P1 | Trypanosoma cruzi | 58% | 99% |