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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H583
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.477 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.754 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.368 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.731 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.642 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.631 |
DOC_CYCLIN_RxL_1 | 13 | 23 | PF00134 | 0.607 |
DOC_CYCLIN_yCln2_LP_2 | 205 | 211 | PF00134 | 0.450 |
DOC_MAPK_gen_1 | 3 | 10 | PF00069 | 0.771 |
DOC_PP2B_LxvP_1 | 205 | 208 | PF13499 | 0.404 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.672 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.817 |
LIG_CtBP_PxDLS_1 | 17 | 21 | PF00389 | 0.607 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.367 |
LIG_LIR_Gen_1 | 158 | 168 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.498 |
LIG_LYPXL_S_1 | 187 | 191 | PF13949 | 0.665 |
LIG_LYPXL_yS_3 | 188 | 191 | PF13949 | 0.422 |
LIG_RPA_C_Fungi | 21 | 33 | PF08784 | 0.499 |
LIG_SH2_CRK | 107 | 111 | PF00017 | 0.378 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 168 | 171 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.490 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.515 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.590 |
LIG_SUMO_SIM_par_1 | 16 | 21 | PF11976 | 0.749 |
LIG_SxIP_EBH_1 | 36 | 49 | PF03271 | 0.577 |
LIG_TRFH_1 | 188 | 192 | PF08558 | 0.410 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.558 |
MOD_CDK_SPK_2 | 11 | 16 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 170 | 175 | PF00069 | 0.466 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.769 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.676 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.500 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.582 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.745 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.691 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.583 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.516 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.697 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.715 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.668 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.705 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.666 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.622 |
MOD_N-GLC_2 | 184 | 186 | PF02516 | 0.513 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.451 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.464 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.667 |
MOD_PKA_1 | 220 | 226 | PF00069 | 0.606 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.589 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.663 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.687 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.675 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.659 |
MOD_PKB_1 | 36 | 44 | PF00069 | 0.585 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.415 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.495 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.550 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.697 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.633 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAL2 | Leptomonas seymouri | 46% | 100% |
A0A1X0NNX7 | Trypanosomatidae | 36% | 88% |
A0A3S7WQ61 | Leishmania donovani | 71% | 100% |
A4HTG7 | Leishmania infantum | 72% | 100% |
E9AM95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QIF3 | Leishmania major | 73% | 100% |