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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6U3
Term | Name | Level | Count |
---|---|---|---|
GO:0006576 | biogenic amine metabolic process | 5 | 7 |
GO:0006595 | polyamine metabolic process | 6 | 7 |
GO:0006596 | polyamine biosynthetic process | 7 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009308 | amine metabolic process | 4 | 7 |
GO:0009309 | amine biosynthetic process | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0042401 | biogenic amine biosynthetic process | 6 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006520 | amino acid metabolic process | 3 | 1 |
GO:0006591 | ornithine metabolic process | 5 | 1 |
GO:0009445 | putrescine metabolic process | 7 | 1 |
GO:0009446 | putrescine biosynthetic process | 8 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0033387 | putrescine biosynthetic process from ornithine | 6 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004586 | ornithine decarboxylase activity | 5 | 6 |
GO:0016829 | lyase activity | 2 | 7 |
GO:0016830 | carbon-carbon lyase activity | 3 | 7 |
GO:0016831 | carboxy-lyase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 289 | 293 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.183 |
CLV_PCSK_FUR_1 | 568 | 572 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.183 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.477 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.507 |
DOC_CYCLIN_RxL_1 | 19 | 29 | PF00134 | 0.616 |
DOC_MAPK_gen_1 | 191 | 198 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 568 | 575 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.414 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.535 |
DOC_PP4_MxPP_1 | 4 | 7 | PF00568 | 0.670 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 474 | 483 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 574 | 581 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 480 | 496 | PF00022 | 0.477 |
LIG_AP2alpha_2 | 230 | 232 | PF02296 | 0.377 |
LIG_BIR_III_2 | 14 | 18 | PF00653 | 0.471 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.477 |
LIG_Clathr_ClatBox_1 | 108 | 112 | PF01394 | 0.427 |
LIG_Clathr_ClatBox_1 | 330 | 334 | PF01394 | 0.418 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.501 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.269 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.477 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.517 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.418 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.477 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.517 |
LIG_LIR_Apic_2 | 301 | 307 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 323 | 331 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 408 | 416 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 443 | 453 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 524 | 535 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 602 | 609 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 625 | 636 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 443 | 449 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 602 | 606 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.314 |
LIG_PCNA_PIPBox_1 | 288 | 297 | PF02747 | 0.418 |
LIG_PCNA_yPIPBox_3 | 261 | 272 | PF02747 | 0.470 |
LIG_PDZ_Class_2 | 631 | 636 | PF00595 | 0.289 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.477 |
LIG_SH2_GRB2like | 521 | 524 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 147 | 151 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 612 | 616 | PF00017 | 0.383 |
LIG_SH2_PTP2 | 324 | 327 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.478 |
LIG_SH3_1 | 225 | 231 | PF00018 | 0.347 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.455 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.389 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.535 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 465 | 471 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 541 | 547 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 328 | 334 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 541 | 547 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 6 | 12 | PF11976 | 0.505 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.510 |
LIG_TYR_ITIM | 322 | 327 | PF00017 | 0.477 |
LIG_UBA3_1 | 330 | 335 | PF00899 | 0.514 |
LIG_WRC_WIRS_1 | 527 | 532 | PF05994 | 0.477 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.447 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.507 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.418 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.381 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.533 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.477 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.477 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.530 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.311 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.285 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.290 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.294 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.490 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.449 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.543 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.480 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.665 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.490 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.438 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.515 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.335 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.227 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.537 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.554 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.477 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.449 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.477 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.518 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.475 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.584 |
MOD_PIKK_1 | 414 | 420 | PF00454 | 0.418 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.431 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.458 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.369 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.376 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.491 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.454 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.559 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.427 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.477 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.477 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.481 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.506 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.495 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.418 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.484 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.414 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.418 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.477 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.477 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.545 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.477 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.477 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.513 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.620 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.470 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.475 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.535 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 568 | 571 | PF00400 | 0.481 |
TRG_NLS_MonoExtC_3 | 23 | 29 | PF00514 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I681 | Leptomonas seymouri | 63% | 88% |
A0A3S5H6K6 | Leishmania donovani | 70% | 90% |
E9AGB5 | Leishmania infantum | 70% | 90% |
E9ANV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 89% |
P27116 | Leishmania donovani | 70% | 90% |
Q4QGR5 | Leishmania major | 70% | 100% |