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. | yes | yes: 25 |
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 |
Related structures:
AlphaFold database: Q4QFX1
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 11 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 11 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 11 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 11 |
GO:0019222 | regulation of metabolic process | 3 | 11 |
GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 2 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 11 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0080090 | regulation of primary metabolic process | 4 | 11 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 2 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 11 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 2 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004402 | histone acetyltransferase activity | 4 | 11 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008080 | N-acetyltransferase activity | 6 | 11 |
GO:0016407 | acetyltransferase activity | 5 | 11 |
GO:0016410 | N-acyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016746 | acyltransferase activity | 3 | 11 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 11 |
GO:0042393 | histone binding | 3 | 2 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140110 | transcription regulator activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.756 |
CLV_PCSK_FUR_1 | 136 | 140 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.756 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.352 |
CLV_PCSK_PC7_1 | 469 | 475 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.551 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.720 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.552 |
DOC_CKS1_1 | 80 | 85 | PF01111 | 0.667 |
DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 290 | 297 | PF00069 | 0.477 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.463 |
DOC_SPAK_OSR1_1 | 376 | 380 | PF12202 | 0.463 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.412 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.793 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.474 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.457 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.599 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.498 |
LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.477 |
LIG_deltaCOP1_diTrp_1 | 161 | 165 | PF00928 | 0.408 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.674 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.553 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.730 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.497 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.463 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.463 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.552 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.547 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.477 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.512 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.536 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.550 |
LIG_GBD_Chelix_1 | 293 | 301 | PF00786 | 0.352 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.399 |
LIG_LIR_Apic_2 | 283 | 288 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 485 | 495 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.635 |
LIG_MLH1_MIPbox_1 | 140 | 144 | PF16413 | 0.512 |
LIG_Pex14_1 | 493 | 497 | PF04695 | 0.509 |
LIG_Pex14_2 | 497 | 501 | PF04695 | 0.591 |
LIG_PTAP_UEV_1 | 515 | 520 | PF05743 | 0.487 |
LIG_PTB_Apo_2 | 17 | 24 | PF02174 | 0.552 |
LIG_REV1ctd_RIR_1 | 141 | 150 | PF16727 | 0.461 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.669 |
LIG_SH3_1 | 502 | 508 | PF00018 | 0.647 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.570 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.471 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.570 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 361 | 367 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.463 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.463 |
LIG_TRFH_1 | 256 | 260 | PF08558 | 0.332 |
LIG_UBA3_1 | 311 | 320 | PF00899 | 0.463 |
MOD_CDK_SPxK_1 | 391 | 397 | PF00069 | 0.463 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.724 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.751 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.547 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.738 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.774 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.536 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.463 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.567 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.675 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.654 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.706 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.597 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.532 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.648 |
MOD_GlcNHglycan | 515 | 519 | PF01048 | 0.553 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.752 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.586 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.385 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.689 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.517 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.746 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.708 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.467 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.552 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.463 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.600 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.438 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.602 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.647 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.740 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.717 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.352 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.786 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.263 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.705 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.579 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.372 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.767 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.501 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.651 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.534 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.451 |
MOD_PKA_1 | 89 | 95 | PF00069 | 0.750 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.660 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.712 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.451 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.750 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.539 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.594 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.463 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.463 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.493 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.399 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.520 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.497 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.643 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.403 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.624 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.463 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.463 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.463 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.790 |
MOD_SUMO_rev_2 | 313 | 322 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 384 | 392 | PF00179 | 0.477 |
TRG_DiLeu_BaEn_1 | 307 | 312 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.490 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 307 | 318 | PF08389 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.263 |
TRG_Pf-PMV_PEXEL_1 | 447 | 452 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B0 | Leptomonas seymouri | 81% | 100% |
A0A1X0NNT9 | Trypanosomatidae | 59% | 100% |
A0A3R7M6T2 | Trypanosoma rangeli | 57% | 100% |
A4H7H5 | Leishmania braziliensis | 88% | 100% |
A4HVV6 | Leishmania infantum | 97% | 100% |
C9ZT70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
D7RTH9 | Leishmania donovani | 97% | 100% |
E9APK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O94446 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
Q2UMQ5 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 100% |
Q4WHG1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 100% |
V5BHR3 | Trypanosoma cruzi | 58% | 100% |