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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGR5
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 2 |
GO:0006520 | amino acid metabolic process | 3 | 2 |
GO:0006576 | biogenic amine metabolic process | 5 | 8 |
GO:0006591 | ornithine metabolic process | 5 | 2 |
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:0009445 | putrescine metabolic process | 7 | 2 |
GO:0009446 | putrescine biosynthetic process | 8 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019752 | carboxylic acid metabolic process | 5 | 2 |
GO:0033387 | putrescine biosynthetic process from ornithine | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0042401 | biogenic amine biosynthetic process | 6 | 8 |
GO:0043436 | oxoacid metabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 8 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 8 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
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:1901605 | alpha-amino acid metabolic process | 4 | 2 |
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 | 396 | 400 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 678 | 680 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.638 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.679 |
CLV_PCSK_PC7_1 | 617 | 623 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.533 |
DEG_APCC_DBOX_1 | 480 | 488 | PF00400 | 0.523 |
DEG_SPOP_SBC_1 | 237 | 241 | PF00917 | 0.511 |
DOC_CYCLIN_RxL_1 | 515 | 526 | PF00134 | 0.486 |
DOC_CYCLIN_RxL_1 | 63 | 73 | PF00134 | 0.649 |
DOC_MAPK_gen_1 | 217 | 224 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 403 | 412 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 403 | 412 | PF00069 | 0.484 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.464 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 391 | 394 | PF00568 | 0.564 |
DOC_PP4_MxPP_1 | 48 | 51 | PF00568 | 0.766 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.499 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.775 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 38 | 46 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 521 | 527 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 625 | 632 | PF00244 | 0.454 |
LIG_14-3-3_CterR_2 | 703 | 707 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 507 | 523 | PF00022 | 0.442 |
LIG_AP2alpha_2 | 257 | 259 | PF02296 | 0.437 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 134 | 138 | PF01394 | 0.524 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.451 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.518 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.578 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.527 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.611 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.738 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.523 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.551 |
LIG_LIR_Apic_2 | 328 | 334 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 388 | 394 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 350 | 358 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 550 | 561 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 653 | 660 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.480 |
LIG_PCNA_yPIPBox_3 | 288 | 299 | PF02747 | 0.515 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.480 |
LIG_Pex14_2 | 609 | 613 | PF04695 | 0.506 |
LIG_Pex14_2 | 670 | 674 | PF04695 | 0.462 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.504 |
LIG_SH2_GRB2like | 547 | 550 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 173 | 177 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.389 |
LIG_SH2_PTP2 | 351 | 354 | PF00017 | 0.523 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 695 | 698 | PF00017 | 0.609 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.556 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.642 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.628 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.469 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.564 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.518 |
LIG_SH3_3 | 601 | 607 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 492 | 498 | PF11976 | 0.523 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 567 | 573 | PF11976 | 0.523 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.566 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.518 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.713 |
LIG_TRAF2_1 | 591 | 594 | PF00917 | 0.496 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.523 |
LIG_UBA3_1 | 373 | 377 | PF00899 | 0.454 |
LIG_WRC_WIRS_1 | 553 | 558 | PF05994 | 0.480 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.561 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.518 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.392 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.623 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.598 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.635 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.480 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.612 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.495 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.460 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.447 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.465 |
MOD_Cter_Amidation | 94 | 97 | PF01082 | 0.609 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.642 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.367 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.302 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.286 |
MOD_GlcNHglycan | 424 | 429 | PF01048 | 0.292 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.305 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.321 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.763 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.332 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.361 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.280 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.718 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.587 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.504 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.703 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.520 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.530 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.473 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.693 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.597 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.323 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.318 |
MOD_N-GLC_2 | 686 | 688 | PF02516 | 0.446 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.524 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.523 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.493 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.529 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.496 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.558 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.681 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.510 |
MOD_NEK2_2 | 516 | 521 | PF00069 | 0.452 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.601 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.557 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.605 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.457 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.518 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.636 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.463 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.513 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.550 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.497 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.598 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.465 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.531 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.523 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.480 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.523 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.523 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.523 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.564 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.496 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.480 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.661 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.583 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.526 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.775 |
TRG_DiLeu_BaLyEn_6 | 67 | 72 | PF01217 | 0.670 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 615 | 617 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 621 | 623 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 677 | 679 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.703 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I681 | Leptomonas seymouri | 62% | 98% |
A0A0S4JJ84 | Bodo saltans | 43% | 100% |
A0A3S5H6K6 | Leishmania donovani | 91% | 100% |
A4H6U3 | Leishmania braziliensis | 70% | 100% |
E9AGB5 | Leishmania infantum | 92% | 100% |
E9ANV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
P27116 | Leishmania donovani | 92% | 100% |