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: A4HS89
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.658 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.689 |
DEG_Kelch_Keap1_1 | 152 | 157 | PF01344 | 0.675 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.639 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.634 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 137 | 144 | PF00244 | 0.628 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.626 |
LIG_EVH1_1 | 169 | 173 | PF00568 | 0.507 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.525 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.665 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.589 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.586 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.695 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.656 |
LIG_IBAR_NPY_1 | 71 | 73 | PF08397 | 0.577 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.688 |
LIG_MYND_1 | 8 | 12 | PF01753 | 0.530 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.555 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.786 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.652 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.496 |
LIG_SH3_1 | 2 | 8 | PF00018 | 0.628 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.669 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.628 |
LIG_SUMO_SIM_par_1 | 126 | 134 | PF11976 | 0.673 |
LIG_TYR_ITSM | 120 | 127 | PF00017 | 0.693 |
LIG_WW_2 | 170 | 173 | PF00397 | 0.507 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.654 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.558 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.681 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.670 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.627 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.694 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.632 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.386 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.651 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.613 |
MOD_LATS_1 | 11 | 17 | PF00433 | 0.537 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.593 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.504 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.617 |
MOD_PK_1 | 13 | 19 | PF00069 | 0.518 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.525 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.624 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.671 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.634 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.575 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.552 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WNW2 | Leishmania donovani | 98% | 100% |
A4H3Z8 | Leishmania braziliensis | 61% | 100% |
O97006 | Leishmania major | 81% | 100% |