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: E9AL31
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.480 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.444 |
CLV_Separin_Metazoa | 183 | 187 | PF03568 | 0.413 |
DEG_SCF_FBW7_1 | 84 | 91 | PF00400 | 0.669 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.668 |
DOC_CYCLIN_RxL_1 | 66 | 75 | PF00134 | 0.404 |
DOC_MAPK_MEF2A_6 | 137 | 145 | PF00069 | 0.481 |
DOC_PP2B_LxvP_1 | 179 | 182 | PF13499 | 0.473 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.528 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.698 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.477 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.529 |
LIG_BIR_III_4 | 19 | 23 | PF00653 | 0.515 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.558 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.658 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.441 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.489 |
LIG_LIR_Apic_2 | 212 | 216 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.520 |
LIG_PDZ_Class_1 | 247 | 252 | PF00595 | 0.583 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.528 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.556 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.464 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.688 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.600 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 108 | 115 | PF11976 | 0.339 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.480 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.709 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.589 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.559 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.627 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.539 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.486 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.503 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.553 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.566 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.525 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.718 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.505 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.617 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.723 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.598 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.622 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.687 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.503 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.625 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.648 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.576 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.511 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.580 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.671 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.515 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.474 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.580 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.503 |
MOD_PKA_1 | 23 | 29 | PF00069 | 0.599 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.652 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.474 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.483 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.514 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.509 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.478 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.475 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.754 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.529 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.633 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.697 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.670 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 132 | 139 | PF00179 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 136 | 141 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.579 |
TRG_ER_FFAT_2 | 208 | 219 | PF00635 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I988 | Leptomonas seymouri | 36% | 100% |
A0A3S5H5W6 | Leishmania donovani | 86% | 100% |
A4H4W5 | Leishmania braziliensis | 61% | 97% |
A4HT39 | Leishmania infantum | 86% | 100% |
Q4QIS3 | Leishmania major | 81% | 100% |