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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AHL9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.633 |
CLV_PCSK_FUR_1 | 105 | 109 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.551 |
CLV_PCSK_PC7_1 | 27 | 33 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.485 |
CLV_Separin_Metazoa | 220 | 224 | PF03568 | 0.646 |
DEG_COP1_1 | 212 | 221 | PF00400 | 0.494 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.678 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.536 |
DOC_MAPK_gen_1 | 117 | 124 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.634 |
DOC_MAPK_RevD_3 | 170 | 185 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 185 | 192 | PF00149 | 0.657 |
DOC_PP1_SILK_1 | 225 | 230 | PF00149 | 0.664 |
DOC_PP2B_LxvP_1 | 263 | 266 | PF13499 | 0.542 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.614 |
DOC_USP7_MATH_2 | 159 | 165 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 107 | 116 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 229 | 236 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 72 | 79 | PF00244 | 0.649 |
LIG_APCC_ABBA_1 | 201 | 206 | PF00400 | 0.648 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.533 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.538 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.493 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.714 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.758 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.719 |
LIG_LIR_LC3C_4 | 206 | 210 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.760 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.720 |
LIG_SH2_PTP2 | 121 | 124 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.755 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.465 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 206 | 214 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 206 | 214 | PF11976 | 0.608 |
LIG_SxIP_EBH_1 | 16 | 27 | PF03271 | 0.513 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.572 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.606 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.703 |
MOD_CDK_SPxxK_3 | 122 | 129 | PF00069 | 0.449 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.644 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.777 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.674 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.588 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.660 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.722 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.602 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.633 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.523 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.737 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.681 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.678 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.754 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.581 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.625 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.742 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.538 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.740 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.675 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.679 |
MOD_N-GLC_2 | 248 | 250 | PF02516 | 0.661 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.598 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.639 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.626 |
MOD_PK_1 | 223 | 229 | PF00069 | 0.661 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.602 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.602 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.530 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.624 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.717 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.605 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.561 |
MOD_Plk_2-3 | 94 | 100 | PF00069 | 0.683 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.518 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.642 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.590 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.637 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.648 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.609 |
MOD_SUMO_rev_2 | 125 | 131 | PF00179 | 0.618 |
MOD_SUMO_rev_2 | 45 | 54 | PF00179 | 0.695 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.629 |
TRG_DiLeu_BaEn_3 | 238 | 244 | PF01217 | 0.750 |
TRG_DiLeu_BaEn_4 | 216 | 222 | PF01217 | 0.632 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.640 |
TRG_NLS_MonoExtN_4 | 184 | 191 | PF00514 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.638 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJH6 | Leptomonas seymouri | 38% | 100% |
A0A3Q8IF41 | Leishmania donovani | 99% | 100% |
A4HJR8 | Leishmania braziliensis | 54% | 100% |
E9B279 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q5X9 | Leishmania major | 83% | 100% |