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: A0A2D1QVA5
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 | 132 | 136 | PF00656 | 0.736 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.821 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.618 |
CLV_MEL_PAP_1 | 389 | 395 | PF00089 | 0.628 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.634 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.761 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.758 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.517 |
CLV_Separin_Metazoa | 575 | 579 | PF03568 | 0.476 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.616 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.606 |
DEG_ODPH_VHL_1 | 403 | 416 | PF01847 | 0.578 |
DEG_SPOP_SBC_1 | 491 | 495 | PF00917 | 0.742 |
DEG_SPOP_SBC_1 | 510 | 514 | PF00917 | 0.509 |
DOC_ANK_TNKS_1 | 178 | 185 | PF00023 | 0.527 |
DOC_ANK_TNKS_1 | 432 | 439 | PF00023 | 0.789 |
DOC_CYCLIN_RxL_1 | 205 | 218 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 363 | 370 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 496 | 502 | PF00069 | 0.759 |
DOC_PP1_RVXF_1 | 565 | 572 | PF00149 | 0.488 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 562 | 565 | PF13499 | 0.500 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 377 | 381 | PF12436 | 0.820 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.825 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 282 | 290 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 44 | 54 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 476 | 486 | PF00244 | 0.834 |
LIG_14-3-3_CanoR_1 | 553 | 560 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.522 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_4 | 135 | 139 | PF00653 | 0.689 |
LIG_eIF4E_1 | 101 | 107 | PF01652 | 0.489 |
LIG_eIF4E_1 | 70 | 76 | PF01652 | 0.577 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.682 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.753 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.751 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.820 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.636 |
LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 163 | 170 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 570 | 577 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.468 |
LIG_NRBOX | 541 | 547 | PF00104 | 0.509 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.389 |
LIG_Pex14_2 | 256 | 260 | PF04695 | 0.506 |
LIG_PTB_Apo_2 | 105 | 112 | PF02174 | 0.623 |
LIG_PTB_Apo_2 | 228 | 235 | PF02174 | 0.574 |
LIG_PTB_Phospho_1 | 105 | 111 | PF10480 | 0.621 |
LIG_Rb_pABgroove_1 | 567 | 575 | PF01858 | 0.468 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.485 |
LIG_SH3_1 | 286 | 292 | PF00018 | 0.633 |
LIG_SH3_1 | 399 | 405 | PF00018 | 0.619 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.562 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.678 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.276 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.546 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.650 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.441 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 413 | 421 | PF11976 | 0.679 |
LIG_SUMO_SIM_par_1 | 413 | 421 | PF11976 | 0.678 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.578 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.534 |
LIG_UBA3_1 | 212 | 217 | PF00899 | 0.546 |
LIG_WW_3 | 302 | 306 | PF00397 | 0.450 |
MOD_CDK_SPxK_1 | 327 | 333 | PF00069 | 0.546 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.546 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.786 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.787 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.706 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.516 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.814 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.822 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.544 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.346 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.703 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.656 |
MOD_GlcNHglycan | 250 | 254 | PF01048 | 0.346 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.837 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.680 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.577 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.739 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.562 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.668 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.812 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.681 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.512 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.692 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.722 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.833 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.772 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.669 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.565 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.711 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.346 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.546 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.755 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.670 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.580 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.552 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.576 |
MOD_NEK2_2 | 438 | 443 | PF00069 | 0.753 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.546 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.716 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.598 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.786 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.574 |
MOD_PKA_1 | 454 | 460 | PF00069 | 0.753 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.763 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.833 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.766 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.556 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.558 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.706 |
MOD_PKB_1 | 454 | 462 | PF00069 | 0.646 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.689 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.475 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.755 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.493 |
MOD_Plk_2-3 | 460 | 466 | PF00069 | 0.822 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.534 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.546 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.475 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.546 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.825 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.706 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 461 | 464 | PF00179 | 0.841 |
MOD_SUMO_rev_2 | 218 | 225 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 373 | 383 | PF00179 | 0.748 |
MOD_SUMO_rev_2 | 431 | 441 | PF00179 | 0.789 |
MOD_SUMO_rev_2 | 457 | 463 | PF00179 | 0.847 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.501 |
TRG_DiLeu_BaEn_4 | 537 | 543 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.633 |
TRG_NLS_MonoExtN_4 | 451 | 458 | PF00514 | 0.754 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIW1 | Leptomonas seymouri | 61% | 81% |
A4HGT1 | Leishmania braziliensis | 79% | 100% |
A4I3V8 | Leishmania infantum | 100% | 100% |
E9B048 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q837 | Leishmania major | 95% | 100% |