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: E9B6X4
Term | Name | Level | Count |
---|---|---|---|
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:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.481 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.481 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.673 |
DEG_SCF_FBW7_1 | 236 | 242 | PF00400 | 0.678 |
DEG_SPOP_SBC_1 | 254 | 258 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.503 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.514 |
DOC_CKS1_1 | 216 | 221 | PF01111 | 0.520 |
DOC_CKS1_1 | 226 | 231 | PF01111 | 0.518 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.673 |
DOC_MAPK_gen_1 | 11 | 20 | PF00069 | 0.459 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.664 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.501 |
DOC_USP7_MATH_2 | 90 | 96 | PF00917 | 0.471 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.710 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.489 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.572 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.446 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.675 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.723 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.612 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.643 |
LIG_Integrin_isoDGR_2 | 191 | 193 | PF01839 | 0.447 |
LIG_LIR_Apic_2 | 250 | 254 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 152 | 163 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.570 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.626 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.609 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.441 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.441 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.598 |
LIG_SH2_SRC | 86 | 89 | PF00017 | 0.642 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.577 |
LIG_SH3_2 | 6 | 11 | PF14604 | 0.456 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.627 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.675 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.578 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.524 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.728 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.679 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.432 |
LIG_TYR_ITSM | 151 | 158 | PF00017 | 0.561 |
LIG_WRC_WIRS_1 | 248 | 253 | PF05994 | 0.542 |
MOD_CDK_SPxxK_3 | 220 | 227 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.465 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.628 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.608 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.483 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.595 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.629 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.542 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.620 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.563 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.643 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.696 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.686 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.545 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.678 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.516 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.539 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.519 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.455 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.724 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.616 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.763 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.605 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.657 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.590 |
MOD_PK_1 | 13 | 19 | PF00069 | 0.465 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.615 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.580 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.503 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.614 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.640 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.660 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.530 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.691 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.553 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.534 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.551 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.682 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.713 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.677 |
TRG_NLS_MonoExtN_4 | 196 | 201 | PF00514 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I468 | Leptomonas seymouri | 30% | 100% |
A0A3S7X9W1 | Leishmania donovani | 85% | 100% |
A4HNB3 | Leishmania braziliensis | 61% | 100% |
A4IBY5 | Leishmania infantum | 85% | 100% |
E9AFS2 | Leishmania major | 85% | 100% |