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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H7H5
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004402 | histone acetyltransferase activity | 4 | 12 |
GO:0008080 | N-acetyltransferase activity | 6 | 12 |
GO:0016407 | acetyltransferase activity | 5 | 12 |
GO:0016410 | N-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 12 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.782 |
CLV_PCSK_FUR_1 | 136 | 140 | PF00082 | 0.719 |
CLV_PCSK_FUR_1 | 470 | 474 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.782 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 472 | 474 | PF00082 | 0.512 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.382 |
CLV_PCSK_PC7_1 | 465 | 471 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.582 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.536 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.778 |
DOC_CDC14_PxL_1 | 487 | 495 | PF14671 | 0.394 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.582 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 286 | 293 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 360 | 363 | PF13499 | 0.496 |
DOC_SPAK_OSR1_1 | 372 | 376 | PF12202 | 0.496 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.530 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.774 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 242 | 257 | PF00022 | 0.310 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.660 |
LIG_BRCT_BRCA1_1 | 140 | 144 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.537 |
LIG_Clathr_ClatBox_1 | 288 | 292 | PF01394 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 161 | 165 | PF00928 | 0.454 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.475 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.604 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.759 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.507 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.507 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.582 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.601 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.552 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.541 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.570 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.620 |
LIG_GBD_Chelix_1 | 289 | 297 | PF00786 | 0.382 |
LIG_LIR_Apic_2 | 161 | 167 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 279 | 284 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 481 | 491 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.536 |
LIG_MLH1_MIPbox_1 | 140 | 144 | PF16413 | 0.597 |
LIG_PTB_Apo_2 | 17 | 24 | PF02174 | 0.582 |
LIG_REV1ctd_RIR_1 | 141 | 150 | PF16727 | 0.538 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 467 | 471 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 483 | 487 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 429 | 432 | PF00017 | 0.507 |
LIG_SH2_STAT3 | 46 | 49 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.351 |
LIG_SH3_1 | 498 | 504 | PF00018 | 0.685 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.503 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 101 | 106 | PF11976 | 0.550 |
LIG_SUMO_SIM_anti_2 | 303 | 309 | PF11976 | 0.507 |
LIG_SUMO_SIM_anti_2 | 357 | 363 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.582 |
LIG_SUMO_SIM_par_1 | 287 | 292 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.496 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.507 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.577 |
LIG_TRFH_1 | 252 | 256 | PF08558 | 0.407 |
LIG_UBA3_1 | 307 | 316 | PF00899 | 0.506 |
MOD_CDK_SPxK_1 | 387 | 393 | PF00069 | 0.496 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.721 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.712 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.601 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.732 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.754 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.570 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.496 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.605 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.650 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.709 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.732 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.699 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.361 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.708 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.627 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.580 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.614 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.721 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.478 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.658 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.597 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.607 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.581 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.496 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.489 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.687 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.638 |
MOD_LATS_1 | 447 | 453 | PF00433 | 0.517 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.382 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.794 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.296 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.736 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.739 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.602 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.394 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.751 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.718 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.649 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.541 |
MOD_PIKK_1 | 512 | 518 | PF00454 | 0.607 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.582 |
MOD_PKA_1 | 89 | 95 | PF00069 | 0.781 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.702 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.751 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.434 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.494 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.781 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.587 |
MOD_PKB_1 | 473 | 481 | PF00069 | 0.337 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.684 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.638 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.496 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.496 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.565 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.561 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.522 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.680 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.454 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.496 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.496 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.496 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.774 |
MOD_SUMO_for_1 | 471 | 474 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 309 | 318 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 380 | 388 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 303 | 314 | PF08389 | 0.537 |
TRG_NLS_MonoExtC_3 | 468 | 473 | PF00514 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 443 | 448 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B0 | Leptomonas seymouri | 79% | 100% |
A0A0S4IZ19 | Bodo saltans | 40% | 100% |
A0A1X0NNT9 | Trypanosomatidae | 58% | 100% |
A0A3R7M6T2 | Trypanosoma rangeli | 59% | 100% |
A4HVV6 | Leishmania infantum | 87% | 100% |
C9ZT70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
D7RTH9 | Leishmania donovani | 87% | 100% |
E9APK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B048 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 68% |
O94446 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
Q2UMQ5 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 30% | 100% |
Q4QFX1 | Leishmania major | 88% | 100% |
Q4WHG1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 100% |
V5BHR3 | Trypanosoma cruzi | 59% | 100% |