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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4H3Z8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.531 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 65 | 73 | PF00400 | 0.515 |
DEG_Kelch_Keap1_1 | 232 | 237 | PF01344 | 0.780 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.464 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.468 |
DOC_CKS1_1 | 54 | 59 | PF01111 | 0.531 |
DOC_MAPK_gen_1 | 66 | 72 | PF00069 | 0.538 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 217 | 224 | PF00244 | 0.677 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.451 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.640 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.706 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.658 |
LIG_LIR_Apic_2 | 132 | 137 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.701 |
LIG_MYND_1 | 160 | 164 | PF01753 | 0.544 |
LIG_MYND_1 | 53 | 57 | PF01753 | 0.525 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.776 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.735 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 103 | 107 | PF00017 | 0.776 |
LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 188 | 191 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.684 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.551 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.694 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.645 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.452 |
LIG_SH3_CIN85_PxpxPR_1 | 57 | 62 | PF14604 | 0.527 |
LIG_SUMO_SIM_par_1 | 206 | 214 | PF11976 | 0.659 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.548 |
LIG_TYR_ITSM | 200 | 207 | PF00017 | 0.697 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.558 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.744 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.650 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.787 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.546 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.453 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.366 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.555 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.603 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.699 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.609 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.604 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.663 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.510 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.668 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.544 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.448 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.604 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.510 |
MOD_NEK2_2 | 87 | 92 | PF00069 | 0.545 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.687 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.558 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.544 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.564 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.439 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.762 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.500 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.537 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.528 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.758 |
MOD_SUMO_rev_2 | 177 | 186 | PF00179 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 50 | 55 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.745 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.540 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.528 |
TRG_NLS_MonoExtC_3 | 65 | 71 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WNW2 | Leishmania donovani | 62% | 100% |
A4HS89 | Leishmania infantum | 61% | 100% |
O97006 | Leishmania major | 62% | 100% |