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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0000811 | GINS complex | 4 | 1 |
GO:0031261 | DNA replication preinitiation complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0032993 | protein-DNA complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9ALJ7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 12 |
GO:0006261 | DNA-templated DNA replication | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.378 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.559 |
CLV_Separin_Metazoa | 153 | 157 | PF03568 | 0.342 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.351 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.582 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.537 |
DOC_MAPK_MEF2A_6 | 135 | 144 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.442 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.522 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 144 | 162 | PF00022 | 0.374 |
LIG_APCC_ABBA_1 | 167 | 172 | PF00400 | 0.261 |
LIG_BIR_III_4 | 18 | 22 | PF00653 | 0.452 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.695 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.733 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.738 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.396 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.714 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.500 |
LIG_NRBOX | 150 | 156 | PF00104 | 0.362 |
LIG_PCNA_yPIPBox_3 | 106 | 119 | PF02747 | 0.497 |
LIG_Rb_LxCxE_1 | 137 | 153 | PF01857 | 0.218 |
LIG_SH2_GRB2like | 305 | 308 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.476 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.475 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.672 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.592 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.399 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 257 | 264 | PF11976 | 0.512 |
LIG_TYR_ITIM | 11 | 16 | PF00017 | 0.521 |
LIG_TYR_ITIM | 169 | 174 | PF00017 | 0.508 |
LIG_WRPW_2 | 308 | 311 | PF00400 | 0.320 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.431 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.685 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.731 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.722 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.393 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.619 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.391 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.435 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.673 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.484 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.413 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.418 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.683 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.660 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.527 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.433 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.487 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.539 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.525 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.668 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.507 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.519 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.696 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.366 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.567 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.532 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.419 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.512 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.511 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.735 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.453 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.462 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.624 |
MOD_Plk_2-3 | 12 | 18 | PF00069 | 0.432 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.450 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.685 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.398 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.424 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.481 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.683 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.235 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.724 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.343 |
TRG_NES_CRM1_1 | 266 | 278 | PF08389 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.735 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I580 | Leptomonas seymouri | 63% | 100% |
A0A0S4IV76 | Bodo saltans | 39% | 100% |
A0A1X0PA08 | Trypanosomatidae | 40% | 100% |
A0A3R7MDL7 | Trypanosoma rangeli | 42% | 100% |
A0A3S7X2T6 | Leishmania donovani | 92% | 100% |
A4HHM6 | Leishmania braziliensis | 78% | 100% |
A4I4U0 | Leishmania infantum | 92% | 100% |
C9ZLI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AE88 | Leishmania major | 92% | 100% |
Q753I0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 100% |
V5DTT2 | Trypanosoma cruzi | 45% | 100% |