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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AFZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
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 | 11 | 13 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.357 |
CLV_Separin_Metazoa | 17 | 21 | PF03568 | 0.489 |
DOC_CDC14_PxL_1 | 227 | 235 | PF14671 | 0.558 |
DOC_CKS1_1 | 125 | 130 | PF01111 | 0.536 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.591 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.472 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 247 | 253 | PF00149 | 0.457 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.523 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.585 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.426 |
LIG_LIR_Gen_1 | 40 | 47 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.394 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.383 |
LIG_SH2_GRB2like | 108 | 111 | PF00017 | 0.565 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 182 | 186 | PF00017 | 0.562 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.506 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.569 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.610 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.577 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.628 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.432 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.760 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.365 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.446 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.528 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.424 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.539 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.542 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.694 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.670 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.416 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.575 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.476 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.598 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.558 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.625 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.438 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.392 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.633 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.325 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.355 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.422 |
MOD_OFUCOSY | 35 | 41 | PF10250 | 0.275 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.552 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.537 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.643 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.577 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.381 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.366 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.382 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.612 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.600 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.586 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.416 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.320 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.583 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.734 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.639 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.389 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.526 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL43 | Leptomonas seymouri | 54% | 90% |
A0A1X0P4Q8 | Trypanosomatidae | 47% | 100% |
A0A3S7XA28 | Leishmania donovani | 93% | 100% |
A4HNI2 | Leishmania braziliensis | 80% | 100% |
A4IC38 | Leishmania infantum | 93% | 100% |
E9B746 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |