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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q4G2
Term | Name | Level | Count |
---|---|---|---|
GO:0007623 | circadian rhythm | 2 | 2 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009416 | response to light stimulus | 4 | 2 |
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009648 | photoperiodism | 5 | 2 |
GO:0009649 | entrainment of circadian clock | 3 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0032501 | multicellular organismal process | 1 | 2 |
GO:0032922 | circadian regulation of gene expression | 2 | 2 |
GO:0042752 | regulation of circadian rhythm | 3 | 2 |
GO:0043153 | entrainment of circadian clock by photoperiod | 4 | 2 |
GO:0048511 | rhythmic process | 1 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0003904 | deoxyribodipyrimidine photo-lyase activity | 5 | 7 |
GO:0003913 | DNA photolyase activity | 4 | 7 |
GO:0005488 | binding | 1 | 2 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016830 | carbon-carbon lyase activity | 3 | 7 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 2 |
GO:0071949 | FAD binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.141 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.206 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.141 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.347 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.493 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.644 |
DOC_CDC14_PxL_1 | 465 | 473 | PF14671 | 0.502 |
DOC_CKS1_1 | 179 | 184 | PF01111 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 222 | 228 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 366 | 374 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 193 | 201 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 24 | 31 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 122 | 129 | PF00149 | 0.460 |
DOC_PP1_RVXF_1 | 300 | 307 | PF00149 | 0.435 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.502 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.412 |
DOC_USP7_UBL2_3 | 354 | 358 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 522 | 526 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 533 | 537 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 268 | 276 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 380 | 387 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 452 | 459 | PF00244 | 0.441 |
LIG_Actin_WH2_2 | 98 | 116 | PF00022 | 0.439 |
LIG_AP2alpha_1 | 77 | 81 | PF02296 | 0.493 |
LIG_BIR_III_2 | 440 | 444 | PF00653 | 0.460 |
LIG_BRCT_BRCA1_1 | 453 | 457 | PF00533 | 0.493 |
LIG_Clathr_ClatBox_1 | 89 | 93 | PF01394 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 407 | 415 | PF00928 | 0.435 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.366 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.401 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.281 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.435 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.460 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 512 | 517 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 174 | 184 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 360 | 367 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 412 | 422 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 447 | 455 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 530 | 535 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.502 |
LIG_PCNA_yPIPBox_3 | 317 | 329 | PF02747 | 0.493 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.435 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.511 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.489 |
LIG_Pex14_2 | 77 | 81 | PF04695 | 0.502 |
LIG_Rb_LxCxE_1 | 243 | 263 | PF01857 | 0.446 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.435 |
LIG_SH2_GRB2like | 350 | 353 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 422 | 426 | PF00017 | 0.451 |
LIG_SH2_SRC | 257 | 260 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.435 |
LIG_SH3_1 | 54 | 60 | PF00018 | 0.457 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.493 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.431 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.476 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.480 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.541 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.486 |
LIG_SUMO_SIM_par_1 | 416 | 421 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.493 |
LIG_TRFH_1 | 161 | 165 | PF08558 | 0.460 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.493 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.460 |
MOD_CDK_SPxxK_3 | 270 | 277 | PF00069 | 0.348 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.502 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.460 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.627 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.529 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.576 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.323 |
MOD_DYRK1A_RPxSP_1 | 5 | 9 | PF00069 | 0.583 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.254 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.606 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.262 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.239 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.386 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.648 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.474 |
MOD_LATS_1 | 275 | 281 | PF00433 | 0.367 |
MOD_LATS_1 | 497 | 503 | PF00433 | 0.421 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.370 |
MOD_N-GLC_2 | 390 | 392 | PF02516 | 0.235 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.383 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.336 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.569 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.460 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.460 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.435 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.460 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.456 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.541 |
MOD_PKA_1 | 499 | 505 | PF00069 | 0.480 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.460 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.460 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.429 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.460 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.454 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.460 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.435 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.482 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.574 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.553 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.493 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.435 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.435 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.348 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.551 |
MOD_SUMO_rev_2 | 118 | 126 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 454 | 464 | PF00179 | 0.493 |
TRG_AP2beta_CARGO_1 | 360 | 369 | PF09066 | 0.493 |
TRG_DiLeu_BaEn_3 | 25 | 31 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 316 | 321 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.341 |
TRG_ER_diLys_1 | 537 | 541 | PF00400 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 114 | 118 | PF00026 | 0.239 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 319 | 324 | PF00026 | 0.293 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT2 | Leptomonas seymouri | 67% | 99% |
A0A1X0P0R5 | Trypanosomatidae | 48% | 97% |
A0A3Q8IEQ0 | Leishmania donovani | 94% | 100% |
A4HL82 | Leishmania braziliensis | 86% | 100% |
A4I8R0 | Leishmania infantum | 94% | 100% |
A9CJC9 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 30% | 100% |
D0A4Q0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 95% |
E9B3M5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O48652 | Arabidopsis thaliana | 24% | 97% |
O77059 | Drosophila melanogaster | 22% | 100% |
P00914 | Escherichia coli (strain K12) | 31% | 100% |
P05066 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 96% |
P05327 | Synechococcus sp. (strain ATCC 27144 / PCC 6301 / SAUG 1402/1) | 30% | 100% |
P12768 | Streptomyces griseus | 32% | 100% |
P25078 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 32% | 100% |
P40115 | Sinapis alba | 28% | 100% |
P57386 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 29% | 100% |
P77967 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 25% | 100% |
P97784 | Mus musculus | 21% | 89% |
Q04449 | Alkalihalophilus pseudofirmus (strain ATCC BAA-2126 / JCM 17055 / OF4) | 30% | 100% |
Q0E2Y1 | Oryza sativa subsp. japonica | 26% | 98% |
Q16526 | Homo sapiens | 22% | 92% |
Q17DK5 | Aedes aegypti | 24% | 99% |
Q293P8 | Drosophila pseudoobscura pseudoobscura | 21% | 100% |
Q32Q86 | Rattus norvegicus | 21% | 92% |
Q38JU2 | Solanum lycopersicum | 26% | 94% |
Q3IPX9 | Natronomonas pharaonis (strain ATCC 35678 / DSM 2160 / CIP 103997 / JCM 8858 / NBRC 14720 / NCIMB 2260 / Gabara) | 26% | 100% |
Q43125 | Arabidopsis thaliana | 27% | 79% |
Q49AN0 | Homo sapiens | 24% | 91% |
Q4KML2 | Danio rerio | 26% | 100% |
Q55081 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 27% | 100% |
Q5IFN2 | Ostreococcus tauri | 25% | 99% |
Q5IZC5 | Erithacus rubecula | 22% | 87% |
Q5QXE0 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 27% | 100% |
Q6ZZY0 | Sylvia borin | 23% | 87% |
Q70AD6 | Spalax judaei | 22% | 92% |
Q75WS4 | Xenopus laevis | 26% | 100% |
Q7NMD1 | Gloeobacter violaceus (strain ATCC 29082 / PCC 7421) | 27% | 100% |
Q7PYI7 | Anopheles gambiae | 25% | 99% |
Q7UJB1 | Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) | 25% | 100% |
Q84KJ5 | Arabidopsis thaliana | 25% | 95% |
Q87JP5 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 25% | 100% |
Q8QG60 | Gallus gallus | 24% | 93% |
Q8QG61 | Gallus gallus | 23% | 87% |
Q8WP19 | Macaca fascicularis | 22% | 92% |
Q923I8 | Rattus norvegicus | 25% | 91% |
Q96524 | Arabidopsis thaliana | 28% | 88% |
Q9HQ46 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 29% | 100% |
Q9KNA8 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 100% |
Q9KR33 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 24% | 100% |
Q9KS67 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 21% | 100% |
Q9R194 | Mus musculus | 25% | 91% |