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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HGT1
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 7 |
GO:0009889 | regulation of biosynthetic process | 4 | 7 |
GO:0010468 | regulation of gene expression | 5 | 7 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 7 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 7 |
GO:0051252 | regulation of RNA metabolic process | 5 | 7 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0080090 | regulation of primary metabolic process | 4 | 7 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 7 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 7 |
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 | 7 |
GO:0004402 | histone acetyltransferase activity | 4 | 7 |
GO:0008080 | N-acetyltransferase activity | 6 | 7 |
GO:0016407 | acetyltransferase activity | 5 | 7 |
GO:0016410 | N-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 7 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
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_C14_Caspase3-7 | 428 | 432 | PF00656 | 0.797 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.735 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.506 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.626 |
DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.581 |
DOC_ANK_TNKS_1 | 149 | 156 | PF00023 | 0.512 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.448 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.297 |
DOC_CYCLIN_RxL_1 | 176 | 189 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 334 | 341 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 498 | 506 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 535 | 542 | PF00149 | 0.479 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.479 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.437 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.788 |
DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.798 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 131 | 137 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 446 | 456 | PF00244 | 0.806 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.522 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 564 | 568 | PF00533 | 0.447 |
LIG_CtBP_PxDLS_1 | 461 | 465 | PF00389 | 0.525 |
LIG_eIF4E_1 | 36 | 42 | PF01652 | 0.596 |
LIG_eIF4E_1 | 67 | 73 | PF01652 | 0.481 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.580 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.816 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 63 | 69 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 134 | 141 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.490 |
LIG_MLH1_MIPbox_1 | 201 | 205 | PF16413 | 0.448 |
LIG_NRBOX | 511 | 517 | PF00104 | 0.497 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.434 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.504 |
LIG_PTB_Apo_2 | 71 | 78 | PF02174 | 0.632 |
LIG_PTB_Phospho_1 | 71 | 77 | PF10480 | 0.629 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 290 | 294 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.459 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.530 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.541 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.518 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.431 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.462 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 384 | 391 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 284 | 289 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 384 | 391 | PF11976 | 0.596 |
LIG_UBA3_1 | 183 | 188 | PF00899 | 0.546 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 95 | 102 | PF00069 | 0.559 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.546 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.757 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.668 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.548 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.532 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.546 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.784 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.813 |
MOD_Cter_Amidation | 251 | 254 | PF01082 | 0.346 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.346 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.601 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.719 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.543 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.783 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.402 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.574 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.566 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.497 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.546 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.685 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.664 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.641 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.294 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.567 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.548 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.346 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.613 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.546 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.464 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.559 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.678 |
MOD_NEK2_2 | 12 | 17 | PF00069 | 0.404 |
MOD_NEK2_2 | 543 | 548 | PF00069 | 0.319 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.546 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.619 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.539 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.702 |
MOD_PK_1 | 257 | 263 | PF00069 | 0.514 |
MOD_PKA_1 | 253 | 259 | PF00069 | 0.717 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.725 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.425 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.702 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.832 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.700 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.530 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.529 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.572 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.680 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.570 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.813 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.415 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.546 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.546 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.360 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.458 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.709 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.693 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.546 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.548 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.812 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.462 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.721 |
MOD_SUMO_for_1 | 432 | 435 | PF00179 | 0.837 |
MOD_SUMO_rev_2 | 189 | 196 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 428 | 434 | PF00179 | 0.829 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_4 | 507 | 513 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.591 |
TRG_NES_CRM1_1 | 161 | 175 | PF08389 | 0.427 |
TRG_NLS_MonoExtC_3 | 424 | 429 | PF00514 | 0.715 |
TRG_NLS_MonoExtN_4 | 425 | 430 | PF00514 | 0.720 |
TRG_Pf-PMV_PEXEL_1 | 279 | 283 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.598 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIW1 | Leptomonas seymouri | 60% | 77% |
A0A2D1QVA5 | Leishmania donovani | 79% | 95% |
A4I3V8 | Leishmania infantum | 79% | 95% |
E9B048 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 74% |
Q4Q837 | Leishmania major | 78% | 100% |