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: A0A3S7X5Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0000122 | negative regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010563 | negative regulation of phosphorus metabolic process | 6 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010921 | regulation of phosphatase activity | 5 | 1 |
GO:0010923 | negative regulation of phosphatase activity | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0035303 | regulation of dephosphorylation | 7 | 1 |
GO:0035305 | negative regulation of dephosphorylation | 8 | 1 |
GO:0043086 | negative regulation of catalytic activity | 4 | 1 |
GO:0044092 | negative regulation of molecular function | 3 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045936 | negative regulation of phosphate metabolic process | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051336 | regulation of hydrolase activity | 4 | 1 |
GO:0051346 | negative regulation of hydrolase activity | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003714 | transcription corepressor activity | 3 | 1 |
GO:0004857 | enzyme inhibitor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019212 | phosphatase inhibitor activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
GO:0140678 | molecular function inhibitor activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.306 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.494 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.506 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.493 |
DEG_SCF_FBW7_1 | 213 | 220 | PF00400 | 0.693 |
DEG_SPOP_SBC_1 | 223 | 227 | PF00917 | 0.682 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.660 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.651 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.589 |
DOC_MAPK_gen_1 | 445 | 453 | PF00069 | 0.555 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.633 |
DOC_PP4_MxPP_1 | 542 | 545 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.485 |
DOC_USP7_MATH_2 | 481 | 487 | PF00917 | 0.548 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.663 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 221 | 231 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 273 | 280 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 490 | 497 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.543 |
LIG_BIR_III_2 | 383 | 387 | PF00653 | 0.620 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.600 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.451 |
LIG_EH1_1 | 507 | 515 | PF00400 | 0.578 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.572 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.700 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.763 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.495 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.573 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.642 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.591 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.466 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.427 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.585 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.435 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.578 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.599 |
LIG_LIR_Apic_2 | 360 | 364 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 16 | 22 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.463 |
LIG_LIR_LC3C_4 | 374 | 377 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.463 |
LIG_MYND_1 | 545 | 549 | PF01753 | 0.574 |
LIG_PCNA_yPIPBox_3 | 135 | 145 | PF02747 | 0.526 |
LIG_PDZ_Class_3 | 565 | 570 | PF00595 | 0.608 |
LIG_PTAP_UEV_1 | 377 | 382 | PF05743 | 0.540 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.648 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 233 | 237 | PF00017 | 0.523 |
LIG_SH2_SRC | 508 | 511 | PF00017 | 0.513 |
LIG_SH2_SRC | 6 | 9 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.574 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.657 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.628 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.713 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.635 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.590 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.463 |
LIG_SH3_4 | 554 | 561 | PF00018 | 0.522 |
LIG_SUMO_SIM_anti_2 | 77 | 84 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 250 | 258 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 77 | 84 | PF11976 | 0.465 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.500 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.670 |
LIG_TYR_ITIM | 231 | 236 | PF00017 | 0.547 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.555 |
MOD_CDK_SPK_2 | 196 | 201 | PF00069 | 0.603 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.801 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.564 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.741 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.725 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.731 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.581 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.594 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.665 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.762 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.422 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.520 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.439 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.605 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.727 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.633 |
MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.272 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.728 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.751 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.552 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.553 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.673 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.589 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.708 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.694 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.744 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.652 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.550 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.611 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.674 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.643 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.685 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.681 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.640 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.265 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.612 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.788 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.686 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.658 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.543 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.650 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.760 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.609 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.712 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.584 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.623 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.306 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.635 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.582 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.506 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.579 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.649 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.463 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.681 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.708 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.527 |
MOD_PK_1 | 556 | 562 | PF00069 | 0.421 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.474 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.580 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.613 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.697 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.705 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.532 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.455 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.599 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.509 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.498 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.548 |
MOD_Plk_2-3 | 247 | 253 | PF00069 | 0.432 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.517 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.671 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.591 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.518 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.506 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.696 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.604 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.622 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.576 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.603 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.671 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.665 |
MOD_SUMO_for_1 | 122 | 125 | PF00179 | 0.500 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 454 | 460 | PF00179 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 563 | 568 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M6 | Leptomonas seymouri | 46% | 100% |
A0A3R7KPD3 | Trypanosoma rangeli | 36% | 100% |
A4HKS5 | Leishmania braziliensis | 70% | 99% |
A4I8A5 | Leishmania infantum | 99% | 100% |
E9B363 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
Q4Q4Z1 | Leishmania major | 89% | 100% |