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: Q4Q4Z1
Term | Name | Level | Count |
---|---|---|---|
GO:0000122 | negative regulation of transcription by RNA polymerase II | 8 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010563 | negative regulation of phosphorus metabolic process | 6 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010921 | regulation of phosphatase activity | 5 | 2 |
GO:0010923 | negative regulation of phosphatase activity | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 2 |
GO:0035303 | regulation of dephosphorylation | 7 | 2 |
GO:0035305 | negative regulation of dephosphorylation | 8 | 2 |
GO:0043086 | negative regulation of catalytic activity | 4 | 2 |
GO:0044092 | negative regulation of molecular function | 3 | 2 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 2 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045936 | negative regulation of phosphate metabolic process | 7 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 2 |
GO:0051336 | regulation of hydrolase activity | 4 | 2 |
GO:0051346 | negative regulation of hydrolase activity | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 2 |
GO:0003712 | transcription coregulator activity | 2 | 2 |
GO:0003714 | transcription corepressor activity | 3 | 2 |
GO:0004857 | enzyme inhibitor activity | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0019208 | phosphatase regulator activity | 3 | 2 |
GO:0019212 | phosphatase inhibitor activity | 4 | 2 |
GO:0030234 | enzyme regulator activity | 2 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 2 |
GO:0140110 | transcription regulator activity | 1 | 2 |
GO:0140678 | molecular function inhibitor activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.530 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 552 | 558 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.572 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.500 |
DEG_SCF_FBW7_1 | 213 | 220 | PF00400 | 0.739 |
DEG_SPOP_SBC_1 | 223 | 227 | PF00917 | 0.660 |
DEG_SPOP_SBC_1 | 404 | 408 | PF00917 | 0.628 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.633 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.590 |
DOC_CYCLIN_RxL_1 | 552 | 564 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 445 | 453 | PF00069 | 0.661 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.615 |
DOC_PP4_MxPP_1 | 542 | 545 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.457 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.644 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 273 | 280 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 304 | 314 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 418 | 428 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 490 | 497 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 505 | 513 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 557 | 561 | PF00244 | 0.536 |
LIG_BIR_III_2 | 383 | 387 | PF00653 | 0.605 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.589 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.438 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.749 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.513 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.605 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.560 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.457 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.472 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.588 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.420 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.618 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 360 | 364 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 16 | 22 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 232 | 240 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.470 |
LIG_MYND_1 | 209 | 213 | PF01753 | 0.547 |
LIG_MYND_1 | 314 | 318 | PF01753 | 0.534 |
LIG_PCNA_yPIPBox_3 | 135 | 145 | PF02747 | 0.516 |
LIG_PDZ_Class_3 | 565 | 570 | PF00595 | 0.608 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.648 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 233 | 237 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.396 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.623 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.613 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.598 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.592 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.598 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.492 |
LIG_SH3_4 | 554 | 561 | PF00018 | 0.584 |
LIG_SH3_CIN85_PxpxPR_1 | 196 | 201 | PF14604 | 0.519 |
LIG_SUMO_SIM_anti_2 | 77 | 84 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 250 | 258 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 544 | 549 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 77 | 84 | PF11976 | 0.465 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.488 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.625 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.537 |
LIG_TYR_ITIM | 231 | 236 | PF00017 | 0.527 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.566 |
MOD_CDK_SPK_2 | 196 | 201 | PF00069 | 0.584 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.758 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.690 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.736 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.503 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.773 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.671 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.647 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.531 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.426 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.522 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.422 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.596 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.715 |
MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.257 |
MOD_DYRK1A_RPxSP_1 | 187 | 191 | PF00069 | 0.513 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.691 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.707 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.693 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.513 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.652 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.563 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.650 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.710 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.675 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.627 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.571 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.542 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.634 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.619 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.670 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.628 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.257 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.704 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.693 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.504 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.684 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.607 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.630 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.630 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.761 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.518 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.661 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.300 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.620 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.527 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.481 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.613 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.591 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.457 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.638 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.697 |
MOD_PKA_1 | 556 | 562 | PF00069 | 0.536 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.528 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.527 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.519 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.582 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.584 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.536 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.684 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.492 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.522 |
MOD_Plk_2-3 | 247 | 253 | PF00069 | 0.415 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.504 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.539 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.644 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.536 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.568 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.500 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.745 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.740 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.723 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.594 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.602 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 122 | 125 | PF00179 | 0.488 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.457 |
TRG_NLS_MonoExtN_4 | 554 | 560 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 563 | 568 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M6 | Leptomonas seymouri | 45% | 100% |
A0A3S7X5Y7 | Leishmania donovani | 89% | 100% |
A4HKS5 | Leishmania braziliensis | 68% | 100% |
A4I8A5 | Leishmania infantum | 89% | 100% |
E9B363 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5BHZ0 | Trypanosoma cruzi | 38% | 100% |