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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000808 | origin recognition complex | 2 | 1 |
GO:0005664 | nuclear origin of replication recognition complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HG46
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006260 | DNA replication | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0006270 | DNA replication initiation | 5 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033314 | mitotic DNA replication checkpoint signaling | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 1 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:0051301 | cell division | 2 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003688 | DNA replication origin binding | 7 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 245 | 251 | PF00089 | 0.354 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.481 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.267 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.390 |
CLV_Separin_Metazoa | 394 | 398 | PF03568 | 0.321 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.369 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.413 |
DOC_CYCLIN_RxL_1 | 185 | 195 | PF00134 | 0.365 |
DOC_CYCLIN_yCln2_LP_2 | 430 | 436 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 5 | 11 | PF00134 | 0.389 |
DOC_MAPK_FxFP_2 | 7 | 10 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.278 |
DOC_MAPK_gen_1 | 220 | 227 | PF00069 | 0.258 |
DOC_MAPK_JIP1_4 | 167 | 173 | PF00069 | 0.176 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 333 | 341 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 423 | 430 | PF00069 | 0.422 |
DOC_MAPK_RevD_3 | 339 | 355 | PF00069 | 0.453 |
DOC_PP1_RVXF_1 | 190 | 197 | PF00149 | 0.258 |
DOC_PP1_RVXF_1 | 322 | 329 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 384 | 390 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.351 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.311 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.385 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.258 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.310 |
DOC_USP7_UBL2_3 | 181 | 185 | PF12436 | 0.266 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.246 |
LIG_14-3-3_CanoR_1 | 278 | 287 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 397 | 402 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 383 | 399 | PF00022 | 0.427 |
LIG_AP2alpha_1 | 321 | 325 | PF02296 | 0.421 |
LIG_BIR_III_4 | 445 | 449 | PF00653 | 0.423 |
LIG_EH1_1 | 413 | 421 | PF00400 | 0.301 |
LIG_eIF4E_1 | 201 | 207 | PF01652 | 0.338 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.358 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.376 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.349 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.424 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.512 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.409 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.213 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.398 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.507 |
LIG_IRF3_LxIS_1 | 47 | 53 | PF10401 | 0.288 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 195 | 202 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 424 | 434 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.460 |
LIG_MAD2 | 192 | 200 | PF02301 | 0.258 |
LIG_PDZ_Class_2 | 452 | 457 | PF00595 | 0.436 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.390 |
LIG_Pex14_2 | 160 | 164 | PF04695 | 0.258 |
LIG_Pex14_2 | 321 | 325 | PF04695 | 0.421 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.556 |
LIG_Rb_LxCxE_1 | 57 | 78 | PF01857 | 0.372 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 201 | 204 | PF00017 | 0.371 |
LIG_SH2_PTP2 | 427 | 430 | PF00017 | 0.318 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.231 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 340 | 345 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 391 | 397 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 306 | 312 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.400 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.518 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.417 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.355 |
LIG_UBA3_1 | 85 | 93 | PF00899 | 0.302 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.430 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.449 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.429 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.264 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.483 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.508 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.358 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.333 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.272 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.307 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.265 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.453 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.466 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.616 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.413 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.448 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.420 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.364 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.648 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.301 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.334 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.294 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.345 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.382 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.483 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.400 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.384 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.449 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.457 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.508 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.450 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.579 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.539 |
MOD_PKB_1 | 29 | 37 | PF00069 | 0.584 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.331 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.471 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.458 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.387 |
MOD_SUMO_rev_2 | 106 | 113 | PF00179 | 0.361 |
MOD_SUMO_rev_2 | 212 | 221 | PF00179 | 0.258 |
MOD_SUMO_rev_2 | 24 | 30 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_1 | 391 | 396 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_4 | 391 | 397 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 275 | 280 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.254 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.448 |
TRG_NES_CRM1_1 | 391 | 403 | PF08389 | 0.322 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M7 | Leptomonas seymouri | 81% | 100% |
A0A1X0NVQ9 | Trypanosomatidae | 54% | 100% |
A0A3S5H7I5 | Leishmania donovani | 87% | 100% |
A0A422NKR1 | Trypanosoma rangeli | 53% | 100% |
A4I376 | Leishmania infantum | 87% | 100% |
D0A7Q2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AZG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4JAS8 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 23% | 100% |
Q4Q8R7 | Leishmania major | 88% | 100% |
Q8W032 | Arabidopsis thaliana | 23% | 90% |
Q975X3 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 24% | 100% |
Q980N4 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 24% | 100% |
V5D7Z4 | Trypanosoma cruzi | 54% | 100% |