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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q837
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 8 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 8 |
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 | 8 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 8 |
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 | 8 |
GO:0019222 | regulation of metabolic process | 3 | 8 |
GO:0031323 | regulation of cellular metabolic process | 4 | 8 |
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 | 8 |
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 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 8 |
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 | 8 |
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 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0080090 | regulation of primary metabolic process | 4 | 8 |
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 | 8 |
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 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004402 | histone acetyltransferase activity | 4 | 8 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008080 | N-acetyltransferase activity | 6 | 8 |
GO:0016407 | acetyltransferase activity | 5 | 8 |
GO:0016410 | N-acyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 8 |
GO:0042393 | histone binding | 3 | 2 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:0140110 | transcription regulator activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.731 |
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.811 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.771 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.598 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.798 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.476 |
CLV_Separin_Metazoa | 577 | 581 | PF03568 | 0.499 |
DEG_APCC_DBOX_1 | 43 | 51 | PF00400 | 0.646 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.614 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 493 | 497 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 512 | 516 | PF00917 | 0.494 |
DOC_ANK_TNKS_1 | 180 | 187 | PF00023 | 0.519 |
DOC_ANK_TNKS_1 | 434 | 441 | PF00023 | 0.767 |
DOC_CYCLIN_RxL_1 | 207 | 220 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 365 | 372 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 498 | 504 | PF00069 | 0.815 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.566 |
DOC_PP1_RVXF_1 | 567 | 574 | PF00149 | 0.504 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 564 | 567 | PF13499 | 0.508 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.517 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.746 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 478 | 488 | PF00244 | 0.812 |
LIG_14-3-3_CanoR_1 | 555 | 562 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.501 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.608 |
LIG_BIR_III_4 | 135 | 139 | PF00653 | 0.691 |
LIG_eIF4E_1 | 101 | 107 | PF01652 | 0.518 |
LIG_eIF4E_1 | 70 | 76 | PF01652 | 0.602 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.686 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.801 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.729 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.747 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.727 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.550 |
LIG_LIR_Apic_2 | 153 | 158 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 165 | 172 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 572 | 579 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.413 |
LIG_NRBOX | 543 | 549 | PF00104 | 0.467 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.452 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.517 |
LIG_PTB_Apo_2 | 105 | 112 | PF02174 | 0.572 |
LIG_PTB_Apo_2 | 230 | 237 | PF02174 | 0.545 |
LIG_PTB_Phospho_1 | 105 | 111 | PF10480 | 0.570 |
LIG_Rb_pABgroove_1 | 569 | 577 | PF01858 | 0.488 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 321 | 325 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 467 | 471 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.306 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.354 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.570 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.693 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.522 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.627 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.482 |
LIG_SUMO_SIM_par_1 | 415 | 423 | PF11976 | 0.628 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.545 |
LIG_UBA3_1 | 214 | 219 | PF00899 | 0.517 |
LIG_WW_3 | 304 | 308 | PF00397 | 0.616 |
MOD_CDK_SPxK_1 | 329 | 335 | PF00069 | 0.517 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.555 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.755 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.765 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.688 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.517 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.791 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.748 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.725 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.522 |
MOD_Cter_Amidation | 282 | 285 | PF01082 | 0.355 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.733 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.319 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.804 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.510 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.551 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.717 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.827 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.555 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.734 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.697 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.636 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.431 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.726 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.536 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.724 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.699 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.610 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.499 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.694 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.317 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.551 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.555 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.808 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.651 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.565 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.523 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.588 |
MOD_NEK2_2 | 440 | 445 | PF00069 | 0.731 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.555 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.675 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.600 |
MOD_PKA_1 | 284 | 290 | PF00069 | 0.770 |
MOD_PKA_1 | 327 | 333 | PF00069 | 0.562 |
MOD_PKA_1 | 456 | 462 | PF00069 | 0.760 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.751 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.814 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.771 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.560 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.573 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.688 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.722 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.515 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.800 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.545 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.505 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.447 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.690 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.624 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.517 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.818 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.621 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.492 |
MOD_SUMO_for_1 | 463 | 466 | PF00179 | 0.822 |
MOD_SUMO_rev_2 | 220 | 227 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 375 | 385 | PF00179 | 0.731 |
MOD_SUMO_rev_2 | 433 | 443 | PF00179 | 0.810 |
MOD_SUMO_rev_2 | 459 | 465 | PF00179 | 0.824 |
TRG_DiLeu_BaEn_4 | 539 | 545 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.595 |
TRG_NLS_MonoExtC_3 | 455 | 460 | PF00514 | 0.698 |
TRG_NLS_MonoExtN_4 | 453 | 460 | PF00514 | 0.707 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIW1 | Leptomonas seymouri | 61% | 81% |
A0A2D1QVA5 | Leishmania donovani | 95% | 100% |
A4HGT1 | Leishmania braziliensis | 78% | 100% |
A4I3V8 | Leishmania infantum | 95% | 100% |
D0A925 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B048 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 78% |