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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0070765 | gamma-secretase complex | 3 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098797 | plasma membrane protein complex | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HV58
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0016485 | protein processing | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0043085 | positive regulation of catalytic activity | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044093 | positive regulation of molecular function | 3 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0051604 | protein maturation | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.576 |
CLV_PCSK_FUR_1 | 25 | 29 | PF00082 | 0.401 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 167 | 173 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.188 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.574 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.364 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.466 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 245 | 251 | PF00134 | 0.358 |
DOC_MAPK_DCC_7 | 121 | 129 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 171 | 179 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 25 | 34 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 61 | 71 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 121 | 129 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 188 | 195 | PF00069 | 0.185 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 324 | 332 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.194 |
DOC_PP1_RVXF_1 | 311 | 317 | PF00149 | 0.536 |
DOC_PP1_RVXF_1 | 377 | 383 | PF00149 | 0.325 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.194 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.358 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.371 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.292 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.426 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.194 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.194 |
LIG_14-3-3_CanoR_1 | 367 | 375 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 394 | 404 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 526 | 534 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 557 | 564 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 634 | 641 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 665 | 671 | PF00244 | 0.612 |
LIG_Actin_WH2_2 | 260 | 278 | PF00022 | 0.358 |
LIG_APCC_ABBA_1 | 127 | 132 | PF00400 | 0.337 |
LIG_APCC_ABBAyCdc20_2 | 126 | 132 | PF00400 | 0.342 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.369 |
LIG_CSL_BTD_1 | 89 | 92 | PF09270 | 0.343 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.194 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.318 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.323 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.460 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.530 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.806 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.662 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.364 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.633 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.191 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 669 | 673 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.191 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 669 | 673 | PF02991 | 0.596 |
LIG_NRBOX | 391 | 397 | PF00104 | 0.386 |
LIG_PCNA_yPIPBox_3 | 635 | 649 | PF02747 | 0.258 |
LIG_Pex14_2 | 400 | 404 | PF04695 | 0.335 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.277 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.619 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.362 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.508 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.669 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.270 |
LIG_Sin3_3 | 600 | 607 | PF02671 | 0.251 |
LIG_SUMO_SIM_anti_2 | 650 | 656 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 140 | 145 | PF11976 | 0.194 |
LIG_SUMO_SIM_par_1 | 248 | 254 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 647 | 653 | PF11976 | 0.275 |
LIG_SUMO_SIM_par_1 | 659 | 664 | PF11976 | 0.410 |
LIG_TRAF2_1 | 484 | 487 | PF00917 | 0.618 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.728 |
LIG_TRFH_1 | 327 | 331 | PF08558 | 0.508 |
LIG_TRFH_1 | 609 | 613 | PF08558 | 0.299 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.310 |
LIG_WRC_WIRS_1 | 256 | 261 | PF05994 | 0.270 |
LIG_WW_3 | 91 | 95 | PF00397 | 0.352 |
MOD_CDC14_SPxK_1 | 91 | 94 | PF00782 | 0.353 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.412 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.370 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.184 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.183 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.326 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.274 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.535 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.563 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.631 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.410 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.581 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.686 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.698 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.641 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.350 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.391 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.649 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.361 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.473 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.481 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.603 |
MOD_GlcNHglycan | 535 | 539 | PF01048 | 0.526 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.500 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.435 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.385 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.575 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.624 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.194 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.194 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.340 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.420 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.375 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.452 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.699 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.568 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.686 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.717 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.410 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.480 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.412 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.384 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.397 |
MOD_N-GLC_1 | 641 | 646 | PF02516 | 0.288 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.194 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.584 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.194 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.355 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.325 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.385 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.552 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.425 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.465 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.352 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.704 |
MOD_NEK2_2 | 470 | 475 | PF00069 | 0.720 |
MOD_NEK2_2 | 500 | 505 | PF00069 | 0.669 |
MOD_OFUCOSY | 112 | 119 | PF10250 | 0.570 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.660 |
MOD_PK_1 | 368 | 374 | PF00069 | 0.369 |
MOD_PKA_1 | 367 | 373 | PF00069 | 0.374 |
MOD_PKA_1 | 557 | 563 | PF00069 | 0.629 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.366 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.194 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.432 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.356 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.373 |
MOD_PKB_1 | 207 | 215 | PF00069 | 0.356 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.587 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.370 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.184 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.402 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.571 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.761 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.288 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.224 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.194 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.185 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.379 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.299 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.365 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.568 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.299 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.224 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.674 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.549 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY04 | Leptomonas seymouri | 42% | 100% |
A0A3S7WRT9 | Leishmania donovani | 99% | 100% |
A4H6T0 | Leishmania braziliensis | 66% | 100% |
E9ANU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4QGS9 | Leishmania major | 88% | 100% |