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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4I1T8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008885 | glutathionylspermidine synthase activity | 5 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 3 |
GO:0016880 | acid-ammonia (or amide) ligase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.304 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.269 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.243 |
CLV_C14_Caspase3-7 | 691 | 695 | PF00656 | 0.391 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 654 | 656 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.289 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.502 |
DOC_ANK_TNKS_1 | 260 | 267 | PF00023 | 0.344 |
DOC_MAPK_gen_1 | 450 | 457 | PF00069 | 0.220 |
DOC_MAPK_gen_1 | 62 | 68 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 689 | 698 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 701 | 709 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 106 | 114 | PF00069 | 0.199 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.220 |
DOC_PP1_RVXF_1 | 419 | 426 | PF00149 | 0.269 |
DOC_PP1_RVXF_1 | 454 | 461 | PF00149 | 0.238 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.238 |
DOC_PP4_MxPP_1 | 343 | 346 | PF00568 | 0.238 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.212 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.212 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.238 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.458 |
DOC_USP7_MATH_2 | 605 | 611 | PF00917 | 0.380 |
DOC_USP7_UBL2_3 | 415 | 419 | PF12436 | 0.269 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.238 |
DOC_USP7_UBL2_3 | 660 | 664 | PF12436 | 0.310 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.245 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.188 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.212 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.280 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 304 | 314 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 508 | 516 | PF00244 | 0.245 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.239 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.474 |
LIG_Clathr_ClatBox_1 | 19 | 23 | PF01394 | 0.366 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 103 | 111 | PF00928 | 0.215 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.235 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.365 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.235 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.238 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.305 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.238 |
LIG_FHA_1 | 685 | 691 | PF00498 | 0.319 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.342 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.340 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.238 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.432 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.358 |
LIG_HCF-1_HBM_1 | 7 | 10 | PF13415 | 0.470 |
LIG_Integrin_isoDGR_2 | 582 | 584 | PF01839 | 0.238 |
LIG_LIR_Apic_2 | 245 | 251 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 108 | 119 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 121 | 126 | PF02991 | 0.178 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 340 | 347 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 405 | 411 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.178 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 675 | 681 | PF02991 | 0.284 |
LIG_MYND_1 | 247 | 251 | PF01753 | 0.331 |
LIG_PCNA_PIPBox_1 | 380 | 389 | PF02747 | 0.220 |
LIG_Pex14_2 | 657 | 661 | PF04695 | 0.294 |
LIG_REV1ctd_RIR_1 | 654 | 664 | PF16727 | 0.330 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.353 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.172 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 506 | 509 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.220 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.212 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.511 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.298 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.252 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.247 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.316 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.401 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.383 |
LIG_SUMO_SIM_anti_2 | 488 | 494 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 478 | 486 | PF11976 | 0.238 |
LIG_TRAF2_1 | 604 | 607 | PF00917 | 0.372 |
LIG_TRFH_1 | 327 | 331 | PF08558 | 0.239 |
LIG_TYR_ITIM | 68 | 73 | PF00017 | 0.357 |
LIG_UBA3_1 | 616 | 620 | PF00899 | 0.374 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.328 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.213 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.212 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.372 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.254 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.238 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.238 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.470 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.466 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.352 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.366 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.338 |
MOD_CMANNOS | 494 | 497 | PF00535 | 0.238 |
MOD_DYRK1A_RPxSP_1 | 106 | 110 | PF00069 | 0.213 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.409 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.291 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.238 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.321 |
MOD_GlcNHglycan | 368 | 372 | PF01048 | 0.285 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.325 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.465 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.382 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.387 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.238 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.345 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.286 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.439 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.383 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.367 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.317 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.412 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.379 |
MOD_N-GLC_2 | 529 | 531 | PF02516 | 0.269 |
MOD_N-GLC_2 | 638 | 640 | PF02516 | 0.392 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.241 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.292 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.269 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.390 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.453 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.386 |
MOD_NEK2_2 | 206 | 211 | PF00069 | 0.301 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.238 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.238 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.238 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.439 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.425 |
MOD_PK_1 | 692 | 698 | PF00069 | 0.368 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.362 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.396 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.238 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.238 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.213 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.389 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.238 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.269 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.450 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.337 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.245 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.188 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.212 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.297 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.328 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.280 |
MOD_SUMO_rev_2 | 59 | 65 | PF00179 | 0.375 |
TRG_DiLeu_LyEn_5 | 332 | 337 | PF01217 | 0.238 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.238 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.215 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y6 | Leptomonas seymouri | 27% | 100% |
A0A0N1PC88 | Leptomonas seymouri | 71% | 100% |
A0A0S4J0Y2 | Bodo saltans | 38% | 82% |
A0A0S4JSQ6 | Bodo saltans | 29% | 100% |
A0A1X0ND08 | Trypanosomatidae | 52% | 100% |
A0A1X0NR71 | Trypanosomatidae | 30% | 100% |
A0A3Q8IGF4 | Leishmania donovani | 28% | 100% |
A0A3Q8IGS6 | Leishmania donovani | 99% | 100% |
A0A3R7LYC7 | Trypanosoma rangeli | 30% | 100% |
A4HFW1 | Leishmania braziliensis | 27% | 92% |
A4I2Z3 | Leishmania infantum | 28% | 100% |
C9ZJE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AXX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AZ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 92% |
O60993 | Crithidia fasciculata | 28% | 100% |
P0AES0 | Escherichia coli (strain K12) | 27% | 100% |
P0AES1 | Shigella flexneri | 27% | 100% |
P90518 | Crithidia fasciculata | 70% | 100% |
Q711P7 | Leishmania major | 28% | 91% |
Q9GT49 | Trypanosoma cruzi (strain CL Brener) | 30% | 100% |
V5ASH7 | Trypanosoma cruzi | 49% | 100% |
V5AYP7 | Trypanosoma cruzi | 31% | 100% |