Metal Binding, CHORD, putative |
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) | yes | yes: 3 |
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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HZ16
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0051298 | centrosome duplication | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.468 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 53 | 55 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.413 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.362 |
DOC_CYCLIN_RxL_1 | 35 | 49 | PF00134 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.492 |
DOC_MAPK_FxFP_2 | 175 | 178 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 48 | 58 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 179 | 187 | PF00069 | 0.607 |
DOC_PP1_RVXF_1 | 274 | 281 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.427 |
DOC_PP2B_LxvP_1 | 183 | 186 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.557 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.497 |
LIG_14-3-3_CanoR_1 | 167 | 176 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.377 |
LIG_Actin_WH2_2 | 91 | 109 | PF00022 | 0.468 |
LIG_APCC_ABBAyCdc20_2 | 132 | 138 | PF00400 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 153 | 157 | PF00928 | 0.446 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.377 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 279 | 287 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.358 |
LIG_Rb_pABgroove_1 | 1 | 9 | PF01858 | 0.294 |
LIG_REV1ctd_RIR_1 | 43 | 52 | PF16727 | 0.433 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.328 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 87 | 92 | PF11976 | 0.454 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.602 |
LIG_TRAF2_2 | 224 | 229 | PF00917 | 0.554 |
LIG_UBA3_1 | 90 | 97 | PF00899 | 0.420 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.396 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.666 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.413 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.389 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.350 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.452 |
MOD_Cter_Amidation | 147 | 150 | PF01082 | 0.278 |
MOD_Cter_Amidation | 204 | 207 | PF01082 | 0.679 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.502 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.590 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.611 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.427 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.562 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.601 |
MOD_N-GLC_2 | 125 | 127 | PF02516 | 0.278 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.372 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.538 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.520 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.446 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.336 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.219 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.538 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.581 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.640 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.405 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.606 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.437 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.529 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.389 |
MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.520 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.389 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 199 | 208 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 223 | 232 | PF00179 | 0.441 |
TRG_DiLeu_BaEn_2 | 278 | 284 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2I9 | Leptomonas seymouri | 67% | 100% |
A0A0S4J9B3 | Bodo saltans | 51% | 98% |
A0A1X0NW45 | Trypanosomatidae | 47% | 97% |
A0A3Q8IAQ6 | Leishmania donovani | 100% | 100% |
A0A3R7MVQ5 | Trypanosoma rangeli | 52% | 99% |
A9YUB1 | Sus scrofa | 28% | 89% |
C9ZIN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 97% |
D4A4T9 | Rattus norvegicus | 28% | 89% |
E9AIN0 | Leishmania braziliensis | 76% | 100% |
E9AUW3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
G5EEI8 | Caenorhabditis elegans | 32% | 92% |
Q29RL2 | Bos taurus | 28% | 89% |
Q462R2 | Sus scrofa | 31% | 86% |
Q4QCL9 | Leishmania major | 92% | 100% |
Q4R7U2 | Macaca fascicularis | 28% | 89% |
Q5RD91 | Pongo abelii | 28% | 89% |
Q5ZML4 | Gallus gallus | 28% | 89% |
Q6EPW7 | Oryza sativa subsp. japonica | 30% | 100% |
Q6NUA0 | Xenopus laevis | 29% | 89% |
Q7T3F7 | Danio rerio | 30% | 87% |
Q9D1P4 | Mus musculus | 28% | 89% |
Q9R000 | Mus musculus | 31% | 85% |
Q9SE33 | Arabidopsis thaliana | 30% | 100% |
Q9UHD1 | Homo sapiens | 28% | 89% |
Q9UKP3 | Homo sapiens | 27% | 85% |
Q9VCC0 | Drosophila melanogaster | 28% | 84% |
V5D8W5 | Trypanosoma cruzi | 49% | 86% |