Polyamine metabolism, ornithine decarboxylase LINJ.12.0100
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: E9AGB5
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 | 233 | 237 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.781 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 617 | 623 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.183 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.546 |
DEG_APCC_DBOX_1 | 480 | 488 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 115 | 119 | PF00917 | 0.591 |
DOC_CYCLIN_RxL_1 | 515 | 526 | PF00134 | 0.536 |
DOC_CYCLIN_RxL_1 | 63 | 73 | PF00134 | 0.699 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 675 | 682 | PF00149 | 0.348 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 391 | 394 | PF00568 | 0.619 |
DOC_PP4_MxPP_1 | 48 | 51 | PF00568 | 0.811 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.523 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.816 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 521 | 527 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 625 | 632 | PF00244 | 0.517 |
LIG_14-3-3_CterR_2 | 703 | 707 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 507 | 523 | PF00022 | 0.464 |
LIG_AP2alpha_2 | 257 | 259 | PF02296 | 0.461 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.546 |
LIG_Clathr_ClatBox_1 | 134 | 138 | PF01394 | 0.501 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.417 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.584 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.555 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.546 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.359 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.619 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.691 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.546 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.576 |
LIG_LIR_Apic_2 | 328 | 334 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 388 | 394 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 350 | 358 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 550 | 561 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 653 | 660 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.546 |
LIG_PCNA_yPIPBox_3 | 288 | 299 | PF02747 | 0.539 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.546 |
LIG_Pex14_2 | 609 | 613 | PF04695 | 0.530 |
LIG_Pex14_2 | 670 | 674 | PF04695 | 0.492 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.465 |
LIG_SH2_GRB2like | 547 | 550 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.646 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.476 |
LIG_SH2_PTP2 | 351 | 354 | PF00017 | 0.546 |
LIG_SH2_SRC | 75 | 78 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.640 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.527 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.662 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.567 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.437 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.555 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 492 | 498 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 567 | 573 | PF11976 | 0.546 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.617 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.563 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.678 |
LIG_TRAF2_1 | 591 | 594 | PF00917 | 0.536 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.546 |
LIG_UBA3_1 | 373 | 377 | PF00899 | 0.525 |
LIG_WRC_WIRS_1 | 553 | 558 | PF05994 | 0.546 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.538 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.638 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.549 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.554 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.563 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.471 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.633 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.626 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.546 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.618 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.528 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.530 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.546 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.504 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.498 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.624 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.674 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.544 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.440 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.408 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.346 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.608 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.339 |
MOD_GlcNHglycan | 424 | 429 | PF01048 | 0.345 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.358 |
MOD_GlcNHglycan | 466 | 470 | PF01048 | 0.337 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.729 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.336 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.369 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.292 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.760 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.650 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.607 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.358 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.714 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.544 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.543 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.476 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.693 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.643 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.352 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.294 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.363 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.533 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.466 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.513 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.546 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.521 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.579 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.730 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.545 |
MOD_NEK2_2 | 516 | 521 | PF00069 | 0.475 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.564 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.503 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.380 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.606 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.475 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.563 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.645 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.475 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.530 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.571 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.521 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.626 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.591 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.489 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.546 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.504 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.550 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.522 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.546 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.504 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.619 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.546 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.546 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.639 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.535 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.620 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.817 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.620 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 615 | 617 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 621 | 623 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 677 | 679 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 690 | 693 | PF00400 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.696 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I681 | Leptomonas seymouri | 63% | 98% |
A0A3S5H6K6 | Leishmania donovani | 99% | 100% |
A4H6U3 | Leishmania braziliensis | 70% | 96% |
E9ANV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
P27116 | Leishmania donovani | 100% | 100% |
Q4QGR5 | Leishmania major | 92% | 100% |