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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: Q4Q676
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.618 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.504 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 168 | 177 | PF00134 | 0.656 |
DOC_MAPK_DCC_7 | 101 | 111 | PF00069 | 0.668 |
DOC_MAPK_RevD_3 | 72 | 86 | PF00069 | 0.558 |
DOC_PP2B_PxIxI_1 | 106 | 112 | PF00149 | 0.780 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.792 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.833 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 25 | 33 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.726 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.666 |
LIG_EH_1 | 180 | 184 | PF12763 | 0.768 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.689 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.752 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.531 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.458 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.479 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.690 |
LIG_IRF3_LxIS_1 | 173 | 180 | PF10401 | 0.654 |
LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.800 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.524 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.731 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.723 |
LIG_SH2_PTP2 | 6 | 9 | PF00017 | 0.549 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 11 | 14 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.712 |
LIG_SH3_1 | 6 | 12 | PF00018 | 0.418 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.418 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.648 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.804 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.689 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.758 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.758 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.825 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.697 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.554 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.358 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.505 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.769 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.756 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.683 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.556 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.627 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.708 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.541 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.784 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.747 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.459 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.467 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.486 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.496 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.687 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.737 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.779 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.695 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.847 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.500 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.412 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.709 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.658 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.516 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.718 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.746 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.749 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.549 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.650 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.433 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.264 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.769 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.507 |
TRG_DiLeu_BaEn_4 | 131 | 137 | PF01217 | 0.754 |
TRG_DiLeu_BaEn_4 | 89 | 95 | PF01217 | 0.726 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.744 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.652 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.761 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.695 |
TRG_NLS_MonoExtC_3 | 83 | 89 | PF00514 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 208 | 213 | PF00026 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFE3 | Leishmania donovani | 79% | 98% |
A4I6W0 | Leishmania infantum | 79% | 98% |
E9AIU6 | Leishmania braziliensis | 50% | 98% |
E9B1Y4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 98% |