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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4IBY5
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
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 | 0.599 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.599 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.666 |
DEG_SCF_FBW7_1 | 236 | 242 | PF00400 | 0.692 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.547 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.524 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.660 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.653 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 212 | PF00134 | 0.581 |
DOC_PP1_RVXF_1 | 123 | 130 | PF00149 | 0.511 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.554 |
DOC_PP4_FxxP_1 | 251 | 254 | PF00568 | 0.678 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.527 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.614 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.697 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.671 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.632 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.670 |
LIG_Integrin_isoDGR_2 | 191 | 193 | PF01839 | 0.569 |
LIG_LIR_Apic_2 | 250 | 254 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 152 | 163 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 256 | 263 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.631 |
LIG_PTB_Apo_2 | 225 | 232 | PF02174 | 0.590 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.632 |
LIG_SH2_CRK | 2 | 6 | PF00017 | 0.613 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.621 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.559 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.559 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.656 |
LIG_SH2_SRC | 86 | 89 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.722 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.617 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.566 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.575 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.699 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.609 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.663 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.468 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.530 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.649 |
LIG_WRC_WIRS_1 | 248 | 253 | PF05994 | 0.629 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.763 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.624 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.657 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.569 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.719 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.514 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.667 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.724 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.596 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.559 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.555 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.631 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.543 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.510 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.550 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.547 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.477 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.506 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.708 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.640 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.751 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.636 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.698 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.567 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.534 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.674 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.602 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.715 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.645 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.690 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.604 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.468 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.673 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.573 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.541 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.691 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.629 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.636 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 2 | 5 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.689 |
TRG_NLS_MonoExtN_4 | 196 | 201 | PF00514 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 200 | 205 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X9W1 | Leishmania donovani | 100% | 100% |
A4HNB3 | Leishmania braziliensis | 64% | 100% |
E9AFS2 | Leishmania major | 89% | 100% |
E9B6X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |