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: E9AFS2
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.580 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.660 |
DEG_SCF_FBW7_1 | 215 | 222 | PF00400 | 0.534 |
DEG_SCF_FBW7_1 | 236 | 242 | PF00400 | 0.684 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.475 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.684 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 212 | PF00134 | 0.565 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.672 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.570 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 49 | 53 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.527 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.683 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.747 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.619 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.669 |
LIG_Integrin_isoDGR_2 | 191 | 193 | PF01839 | 0.452 |
LIG_LIR_Apic_2 | 249 | 254 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 152 | 163 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.579 |
LIG_PTB_Apo_2 | 225 | 232 | PF02174 | 0.584 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.637 |
LIG_SH2_CRK | 2 | 6 | PF00017 | 0.608 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.609 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.446 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.446 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.600 |
LIG_SH2_SRC | 86 | 89 | PF00017 | 0.648 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.557 |
LIG_SH3_2 | 163 | 168 | PF14604 | 0.554 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.628 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.672 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.538 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.690 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.601 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.738 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.431 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.579 |
LIG_TYR_ITSM | 151 | 158 | PF00017 | 0.568 |
LIG_WRC_WIRS_1 | 248 | 253 | PF05994 | 0.553 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.626 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.677 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.605 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.635 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.511 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.627 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.653 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.536 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.666 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.733 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.625 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.666 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.541 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.620 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.499 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.585 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.685 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.529 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.554 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.526 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.583 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.721 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.769 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.651 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.566 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.511 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.550 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.523 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.609 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.611 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.581 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.627 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.640 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.669 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.695 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.560 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.557 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.675 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.722 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.678 |
TRG_NLS_MonoExtN_4 | 196 | 201 | PF00514 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 200 | 205 | PF00026 | 0.454 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I468 | Leptomonas seymouri | 31% | 100% |
A0A3S7X9W1 | Leishmania donovani | 89% | 100% |
A4HNB3 | Leishmania braziliensis | 63% | 100% |
A4IBY5 | Leishmania infantum | 89% | 100% |
E9B6X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |