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: E9B363
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 | 334 | 338 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.275 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.275 |
CLV_PCSK_FUR_1 | 543 | 547 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 543 | 549 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.252 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.476 |
DEG_COP1_1 | 309 | 318 | PF00400 | 0.495 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.461 |
DEG_SCF_FBW7_1 | 203 | 210 | PF00400 | 0.682 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.564 |
DEG_SPOP_SBC_1 | 213 | 217 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 307 | 311 | PF00917 | 0.460 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.664 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.580 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.588 |
DOC_CYCLIN_RxL_1 | 543 | 555 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 302 | 308 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 294 | 303 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 436 | 443 | PF00069 | 0.673 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.451 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.629 |
DOC_PP4_MxPP_1 | 533 | 536 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.477 |
DOC_USP7_UBL2_3 | 545 | 549 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 263 | 270 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 412 | 420 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 463 | 471 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 480 | 487 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 495 | 499 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 546 | 552 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.400 |
LIG_BIR_III_2 | 373 | 377 | PF00653 | 0.618 |
LIG_Clathr_ClatBox_1 | 244 | 248 | PF01394 | 0.449 |
LIG_EH1_1 | 497 | 505 | PF00400 | 0.594 |
LIG_EVH1_2 | 535 | 539 | PF00568 | 0.497 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.539 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.401 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.601 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.624 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.475 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.636 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.595 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.475 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.583 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.612 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.448 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.693 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.593 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.529 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.520 |
LIG_LIR_Gen_1 | 16 | 22 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 222 | 230 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.475 |
LIG_MYND_1 | 199 | 203 | PF01753 | 0.563 |
LIG_MYND_1 | 304 | 308 | PF01753 | 0.514 |
LIG_MYND_1 | 536 | 540 | PF01753 | 0.575 |
LIG_PCNA_yPIPBox_3 | 135 | 145 | PF02747 | 0.471 |
LIG_PDZ_Class_3 | 556 | 561 | PF00595 | 0.569 |
LIG_PTAP_UEV_1 | 367 | 372 | PF05743 | 0.530 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.588 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.692 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.500 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.622 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.585 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 77 | 84 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 240 | 248 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 77 | 84 | PF11976 | 0.475 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.770 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.480 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.509 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.680 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.705 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.602 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.660 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.663 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.563 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.532 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.467 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.523 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.671 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.507 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.465 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.690 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.614 |
MOD_Cter_Amidation | 343 | 346 | PF01082 | 0.496 |
MOD_Cter_Amidation | 434 | 437 | PF01082 | 0.487 |
MOD_Cter_Amidation | 99 | 102 | PF01082 | 0.275 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.627 |
MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.602 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.605 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.670 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.546 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.591 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.530 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.620 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.659 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.511 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.660 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.598 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.518 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.610 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.638 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.568 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.610 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.275 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.566 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.689 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.647 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.684 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.529 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.579 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.643 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.603 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.654 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.540 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.548 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.617 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.275 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.619 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.523 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.475 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.655 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.475 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.629 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.506 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.400 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.486 |
MOD_PKA_1 | 547 | 553 | PF00069 | 0.548 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.486 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.559 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.552 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.526 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.616 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.580 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.550 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.576 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.471 |
MOD_Plk_2-3 | 237 | 243 | PF00069 | 0.492 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.529 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.506 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.654 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.581 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.475 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.677 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.667 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.595 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.588 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.568 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.598 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.484 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.475 |
TRG_NLS_MonoCore_2 | 544 | 549 | PF00514 | 0.491 |
TRG_NLS_MonoExtC_3 | 544 | 549 | PF00514 | 0.491 |
TRG_NLS_MonoExtN_4 | 543 | 550 | PF00514 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 554 | 559 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8M6 | Leptomonas seymouri | 46% | 100% |
A0A3S7X5Y7 | Leishmania donovani | 83% | 98% |
A4HKS5 | Leishmania braziliensis | 69% | 99% |
A4I8A5 | Leishmania infantum | 83% | 98% |
Q4Q4Z1 | Leishmania major | 82% | 100% |