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: A4HHM6
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_NRD_NRD_1 | 159 | 161 | PF00675 | 0.326 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.374 |
CLV_Separin_Metazoa | 153 | 157 | PF03568 | 0.293 |
DEG_APCC_DBOX_1 | 155 | 163 | PF00400 | 0.300 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.546 |
DEG_SCF_FBW7_1 | 54 | 61 | PF00400 | 0.566 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.368 |
DOC_MAPK_MEF2A_6 | 135 | 144 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.405 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.414 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 164 | 171 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.435 |
LIG_Actin_WH2_2 | 144 | 162 | PF00022 | 0.326 |
LIG_Actin_WH2_2 | 277 | 295 | PF00022 | 0.356 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.438 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.356 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.601 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.715 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.370 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.480 |
LIG_NRBOX | 150 | 156 | PF00104 | 0.314 |
LIG_PCNA_yPIPBox_3 | 110 | 119 | PF02747 | 0.440 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.448 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.410 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.471 |
LIG_SUMO_SIM_anti_2 | 257 | 264 | PF11976 | 0.457 |
LIG_TYR_ITIM | 169 | 174 | PF00017 | 0.376 |
LIG_WRPW_2 | 308 | 311 | PF00400 | 0.425 |
MOD_CDK_SPK_2 | 213 | 218 | PF00069 | 0.385 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.356 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.683 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.721 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.719 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.349 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.504 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.453 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.390 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.673 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.463 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.396 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.317 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.671 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.573 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.452 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.316 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.619 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.492 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.502 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.638 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.570 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.486 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.492 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.499 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.453 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.601 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.323 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.413 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.347 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.264 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.694 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.591 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.693 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.406 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.476 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.356 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.393 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.378 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.517 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.465 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.415 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.465 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.624 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.293 |
TRG_NES_CRM1_1 | 266 | 278 | PF08389 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I580 | Leptomonas seymouri | 62% | 100% |
A0A0S4IV76 | Bodo saltans | 36% | 100% |
A0A1X0PA08 | Trypanosomatidae | 40% | 100% |
A0A3R7MDL7 | Trypanosoma rangeli | 46% | 100% |
A0A3S7X2T6 | Leishmania donovani | 80% | 100% |
A2VE40 | Bos taurus | 23% | 100% |
A4I4U0 | Leishmania infantum | 79% | 100% |
C9ZLI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AE88 | Leishmania major | 81% | 100% |
E9ALJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q753I0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
V5DTT2 | Trypanosoma cruzi | 46% | 100% |