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: A0A3Q8I9J1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.628 |
CLV_PCSK_PC7_1 | 135 | 141 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.626 |
DOC_ANK_TNKS_1 | 177 | 184 | PF00023 | 0.496 |
DOC_CKS1_1 | 54 | 59 | PF01111 | 0.533 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.604 |
DOC_MAPK_MEF2A_6 | 178 | 186 | PF00069 | 0.468 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.583 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.618 |
LIG_APCC_ABBA_1 | 230 | 235 | PF00400 | 0.510 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.620 |
LIG_EVH1_1 | 81 | 85 | PF00568 | 0.601 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.567 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.481 |
LIG_LIR_Gen_1 | 159 | 167 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.514 |
LIG_PTB_Apo_2 | 125 | 132 | PF02174 | 0.515 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.449 |
LIG_SH2_GRB2like | 160 | 163 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.613 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.556 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.722 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.598 |
LIG_SUMO_SIM_anti_2 | 3 | 8 | PF11976 | 0.557 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.578 |
MOD_CDK_SPxK_1 | 53 | 59 | PF00069 | 0.608 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.746 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.689 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.657 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.444 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.612 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.611 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.608 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.688 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.518 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.470 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.525 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.706 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.710 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.587 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.494 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.634 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.606 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.473 |
MOD_OFUCOSY | 103 | 109 | PF10250 | 0.548 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.650 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.628 |
MOD_PKB_1 | 74 | 82 | PF00069 | 0.626 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.566 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.642 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.688 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.515 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.715 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.657 |
MOD_SUMO_rev_2 | 114 | 124 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 58 | 68 | PF00179 | 0.567 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.639 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ69 | Leptomonas seymouri | 59% | 100% |
A4H726 | Leishmania braziliensis | 78% | 100% |
A4HVF5 | Leishmania infantum | 97% | 100% |
E9AP53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QGD5 | Leishmania major | 94% | 100% |