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 |
Related structures:
AlphaFold database: E9AYJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.796 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.793 |
CLV_PCSK_PC7_1 | 116 | 122 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.515 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.648 |
DOC_CDC14_PxL_1 | 158 | 166 | PF14671 | 0.607 |
DOC_CKS1_1 | 168 | 173 | PF01111 | 0.675 |
DOC_CYCLIN_yCln2_LP_2 | 145 | 148 | PF00134 | 0.667 |
DOC_MAPK_gen_1 | 211 | 218 | PF00069 | 0.644 |
DOC_MAPK_MEF2A_6 | 211 | 218 | PF00069 | 0.644 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.626 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.670 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 71 | 81 | PF00244 | 0.593 |
LIG_APCC_ABBA_1 | 241 | 246 | PF00400 | 0.580 |
LIG_BIR_III_4 | 197 | 201 | PF00653 | 0.639 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.470 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.574 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.684 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.542 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.655 |
LIG_LIR_Apic_2 | 142 | 147 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.648 |
LIG_PCNA_yPIPBox_3 | 62 | 73 | PF02747 | 0.635 |
LIG_Pex14_1 | 122 | 126 | PF04695 | 0.564 |
LIG_REV1ctd_RIR_1 | 106 | 114 | PF16727 | 0.598 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.645 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.657 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.646 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.421 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.688 |
LIG_SxIP_EBH_1 | 156 | 167 | PF03271 | 0.684 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.644 |
LIG_UBA3_1 | 53 | 62 | PF00899 | 0.650 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.687 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.572 |
MOD_CDC14_SPxK_1 | 12 | 15 | PF00782 | 0.671 |
MOD_CDK_SPxK_1 | 9 | 15 | PF00069 | 0.673 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.587 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.635 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.763 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.400 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.694 |
MOD_Cter_Amidation | 118 | 121 | PF01082 | 0.553 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.581 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.688 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.565 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.579 |
MOD_GlcNHglycan | 220 | 225 | PF01048 | 0.556 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.577 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.517 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.664 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.572 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.750 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.673 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.777 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.704 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.629 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.659 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.675 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.552 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.733 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.570 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.549 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.631 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.657 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.667 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.646 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.554 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.497 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.675 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.679 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.685 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.622 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.671 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.724 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA87 | Leptomonas seymouri | 73% | 100% |
A0A0S4J0K3 | Bodo saltans | 37% | 100% |
A0A1X0P8R4 | Trypanosomatidae | 41% | 88% |
A0A3R7JYN8 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X040 | Leishmania donovani | 92% | 100% |
A4HF57 | Leishmania braziliensis | 76% | 100% |
A4I2E1 | Leishmania infantum | 92% | 100% |
C9ZX66 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 93% |
Q4Q8X9 | Leishmania major | 92% | 100% |
V5BA09 | Trypanosoma cruzi | 39% | 84% |