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: E9ATH2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.562 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.515 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 113 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 264 | 272 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.487 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.468 |
DOC_SPAK_OSR1_1 | 166 | 170 | PF12202 | 0.569 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.580 |
DOC_USP7_MATH_2 | 253 | 259 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 37 | 42 | PF00244 | 0.522 |
LIG_CaM_NSCaTE_8 | 95 | 102 | PF13499 | 0.607 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.485 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.522 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.534 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.692 |
LIG_LIR_Apic_2 | 42 | 48 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 174 | 184 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 268 | 274 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 46 | 55 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.582 |
LIG_MYND_1 | 160 | 164 | PF01753 | 0.574 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.468 |
LIG_PTB_Apo_2 | 169 | 176 | PF02174 | 0.443 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.442 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 11 | 15 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.540 |
LIG_SH3_2 | 161 | 166 | PF14604 | 0.488 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.725 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.532 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 40 | 46 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 86 | 91 | PF11976 | 0.569 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.522 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.635 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.505 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.662 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.580 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.580 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.714 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.524 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.511 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.544 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.461 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.733 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.593 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.696 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.811 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.590 |
MOD_GlcNHglycan | 51 | 55 | PF01048 | 0.645 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.649 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.618 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.425 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.536 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.605 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.657 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.725 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.507 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.527 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.446 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.551 |
MOD_OFUCOSY | 118 | 125 | PF10250 | 0.442 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.737 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.506 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.619 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.685 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.453 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.711 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.655 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 31 | 34 | PF00400 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6L2 | Leptomonas seymouri | 41% | 100% |
A0A3Q8IL86 | Leishmania donovani | 84% | 100% |
A4HPQ7 | Leishmania braziliensis | 69% | 99% |
A4ID06 | Leishmania infantum | 84% | 100% |
Q4Q125 | Leishmania major | 84% | 100% |