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:0000439 | transcription factor TFIIH core complex | 4 | 12 |
GO:0005667 | transcription regulator complex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005675 | transcription factor TFIIH holo complex | 4 | 1 |
GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 1 |
GO:1902911 | protein kinase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4ICQ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006289 | nucleotide-excision repair | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 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:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 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:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0006468 | protein phosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070816 | obsolete phosphorylation of RNA polymerase II C-terminal domain | 6 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001671 | ATPase activator activity | 3 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
GO:0140677 | molecular function activator activity | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.466 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.269 |
DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.545 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.497 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.398 |
DOC_CYCLIN_RxL_1 | 113 | 122 | PF00134 | 0.587 |
DOC_CYCLIN_RxL_1 | 232 | 240 | PF00134 | 0.413 |
DOC_MAPK_FxFP_2 | 278 | 281 | PF00069 | 0.417 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 496 | 503 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 551 | 554 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.597 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.663 |
DOC_PP4_FxxP_1 | 278 | 281 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.683 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.220 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 417 | 422 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 510 | 520 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 70 | 79 | PF00244 | 0.487 |
LIG_Actin_WH2_2 | 149 | 166 | PF00022 | 0.477 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 315 | 319 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.747 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.530 |
LIG_CaM_IQ_9 | 41 | 57 | PF13499 | 0.589 |
LIG_CtBP_PxDLS_1 | 330 | 334 | PF00389 | 0.437 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.481 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.489 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.427 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.423 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.667 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.509 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.556 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.688 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.717 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.649 |
LIG_HCF-1_HBM_1 | 77 | 80 | PF13415 | 0.349 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 215 | 221 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 537 | 548 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.513 |
LIG_LIR_LC3C_4 | 478 | 482 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.469 |
LIG_LYPXL_S_1 | 302 | 306 | PF13949 | 0.344 |
LIG_LYPXL_yS_3 | 303 | 306 | PF13949 | 0.344 |
LIG_NRBOX | 260 | 266 | PF00104 | 0.344 |
LIG_NRBOX | 62 | 68 | PF00104 | 0.525 |
LIG_PCNA_PIPBox_1 | 517 | 526 | PF02747 | 0.567 |
LIG_PCNA_yPIPBox_3 | 181 | 189 | PF02747 | 0.415 |
LIG_PCNA_yPIPBox_3 | 224 | 237 | PF02747 | 0.475 |
LIG_PCNA_yPIPBox_3 | 510 | 524 | PF02747 | 0.566 |
LIG_SH2_CRK | 540 | 544 | PF00017 | 0.466 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.570 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.552 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.406 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.377 |
LIG_SUMO_SIM_anti_2 | 234 | 240 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 148 | 153 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 328 | 334 | PF11976 | 0.437 |
LIG_TRFH_1 | 145 | 149 | PF08558 | 0.601 |
LIG_TRFH_1 | 313 | 317 | PF08558 | 0.340 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.385 |
LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.455 |
LIG_UBA3_1 | 374 | 383 | PF00899 | 0.262 |
LIG_WW_3 | 203 | 207 | PF00397 | 0.359 |
MOD_CDC14_SPxK_1 | 458 | 461 | PF00782 | 0.642 |
MOD_CDK_SPK_2 | 455 | 460 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 455 | 462 | PF00069 | 0.548 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.426 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.423 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.659 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.443 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.364 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.720 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.717 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.399 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.612 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.428 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.559 |
MOD_Cter_Amidation | 46 | 49 | PF01082 | 0.494 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.420 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.423 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.350 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.691 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.674 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.595 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.462 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.449 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.369 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.689 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.700 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.475 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.553 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.668 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.456 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.477 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.435 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.406 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.384 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.381 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.356 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.771 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.561 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.663 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.671 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.523 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.662 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.533 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.529 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.340 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.337 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.621 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.400 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.479 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.328 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.480 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.549 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.612 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.375 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.417 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.342 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.220 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.759 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 382 | 385 | PF00179 | 0.262 |
MOD_SUMO_rev_2 | 307 | 313 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 459 | 462 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7V5 | Leptomonas seymouri | 64% | 100% |
A0A0S4JS94 | Bodo saltans | 29% | 100% |
A0A1X0P966 | Trypanosomatidae | 42% | 100% |
A0A3S5H816 | Leishmania donovani | 100% | 100% |
A0A422NK89 | Trypanosoma rangeli | 44% | 100% |
A4HNU0 | Leishmania braziliensis | 81% | 100% |
D0A2Q5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ASK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q1Z6 | Leishmania major | 93% | 100% |
V5B9Y1 | Trypanosoma cruzi | 44% | 100% |