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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANV5
Term | Name | Level | Count |
---|---|---|---|
GO:0006576 | biogenic amine metabolic process | 5 | 8 |
GO:0006595 | polyamine metabolic process | 6 | 8 |
GO:0006596 | polyamine biosynthetic process | 7 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009308 | amine metabolic process | 4 | 8 |
GO:0009309 | amine biosynthetic process | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0042401 | biogenic amine biosynthetic process | 6 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044249 | cellular biosynthetic process | 3 | 8 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
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 | 8 |
GO:0004586 | ornithine decarboxylase activity | 5 | 6 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016830 | carbon-carbon lyase activity | 3 | 8 |
GO:0016831 | carboxy-lyase activity | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 584 | 588 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 686 | 688 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.203 |
CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 652 | 654 | PF00082 | 0.203 |
CLV_PCSK_PC7_1 | 626 | 632 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.609 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 489 | 497 | PF00400 | 0.508 |
DOC_CYCLIN_RxL_1 | 524 | 535 | PF00134 | 0.454 |
DOC_CYCLIN_RxL_1 | 66 | 73 | PF00134 | 0.565 |
DOC_MAPK_gen_1 | 242 | 249 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 487 | 496 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 651 | 660 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 487 | 496 | PF00069 | 0.389 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 608 | 611 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 664 | 667 | PF13499 | 0.450 |
DOC_PP4_FxxP_1 | 340 | 343 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.523 |
DOC_PP4_MxPP_1 | 48 | 51 | PF00568 | 0.692 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 297 | 301 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 510 | 519 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 624 | 629 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 634 | 641 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 516 | 532 | PF00022 | 0.419 |
LIG_AP2alpha_2 | 266 | 268 | PF02296 | 0.417 |
LIG_BRCT_BRCA1_1 | 396 | 400 | PF00533 | 0.465 |
LIG_Clathr_ClatBox_1 | 159 | 163 | PF01394 | 0.472 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.528 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.364 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.461 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.487 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.466 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.508 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.482 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.611 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.389 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.508 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.371 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.465 |
LIG_LIR_Apic_2 | 397 | 403 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 359 | 367 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 480 | 489 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 559 | 570 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 662 | 669 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 685 | 696 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 551 | 556 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 662 | 666 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.302 |
LIG_Pex14_2 | 396 | 400 | PF04695 | 0.465 |
LIG_Pex14_2 | 618 | 622 | PF04695 | 0.491 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.451 |
LIG_SH2_GRB2like | 556 | 559 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 672 | 676 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 360 | 363 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 672 | 676 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.655 |
LIG_SH3_1 | 626 | 632 | PF00018 | 0.389 |
LIG_SH3_2 | 629 | 634 | PF14604 | 0.389 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.534 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.618 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.510 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.437 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.523 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.559 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.398 |
LIG_SUMO_SIM_anti_2 | 501 | 507 | PF11976 | 0.508 |
LIG_SUMO_SIM_anti_2 | 576 | 582 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 490 | 495 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 576 | 582 | PF11976 | 0.508 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.486 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.565 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.656 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.508 |
LIG_WRC_WIRS_1 | 562 | 567 | PF05994 | 0.465 |
MOD_CDC14_SPxK_1 | 41 | 44 | PF00782 | 0.486 |
MOD_CDK_SPK_2 | 82 | 87 | PF00069 | 0.505 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.487 |
MOD_CDK_SPxxK_3 | 38 | 45 | PF00069 | 0.488 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.514 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.518 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.636 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.442 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.533 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.487 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.371 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.524 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.585 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.495 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.613 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.465 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.475 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.431 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.450 |
MOD_Cter_Amidation | 94 | 97 | PF01082 | 0.569 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.641 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.606 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.593 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.345 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.287 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.267 |
MOD_GlcNHglycan | 433 | 438 | PF01048 | 0.280 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.310 |
MOD_GlcNHglycan | 475 | 479 | PF01048 | 0.329 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.743 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.254 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.730 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.710 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.549 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.532 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.674 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.389 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.501 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.521 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.433 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.675 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.590 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.308 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.242 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.246 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.287 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.513 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.508 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.465 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.481 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.546 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.517 |
MOD_NEK2_2 | 525 | 530 | PF00069 | 0.430 |
MOD_NEK2_2 | 708 | 713 | PF00069 | 0.614 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.509 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.533 |
MOD_PK_1 | 634 | 640 | PF00069 | 0.389 |
MOD_PKA_1 | 242 | 248 | PF00069 | 0.425 |
MOD_PKA_1 | 624 | 630 | PF00069 | 0.487 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.598 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.432 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.389 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.508 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.389 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.537 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.482 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.540 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.474 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.491 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.446 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.508 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.508 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.591 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.508 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.508 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.496 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.398 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.481 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.465 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.528 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.688 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.606 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.527 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.511 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.540 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.661 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 629 | 631 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 686 | 688 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 699 | 702 | PF00400 | 0.533 |
TRG_NLS_MonoExtN_4 | 42 | 48 | PF00514 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I681 | Leptomonas seymouri | 63% | 99% |
A0A0S4JJ84 | Bodo saltans | 43% | 100% |
A0A3S5H6K6 | Leishmania donovani | 83% | 100% |
A4H6U3 | Leishmania braziliensis | 69% | 96% |
E9AGB5 | Leishmania infantum | 83% | 100% |
P27116 | Leishmania donovani | 83% | 100% |
Q4QGR5 | Leishmania major | 82% | 96% |