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: 9 |
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:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AD07
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 2 |
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006631 | fatty acid metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019541 | propionate metabolic process | 6 | 2 |
GO:0019678 | propionate metabolic process, methylmalonyl pathway | 7 | 2 |
GO:0019752 | carboxylic acid metabolic process | 5 | 2 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 2 |
GO:0043436 | oxoacid metabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0046459 | short-chain fatty acid metabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004494 | methylmalonyl-CoA mutase activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016853 | isomerase activity | 2 | 8 |
GO:0016866 | intramolecular transferase activity | 3 | 8 |
GO:0019842 | vitamin binding | 3 | 8 |
GO:0031419 | cobalamin binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0046906 | tetrapyrrole binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.457 |
CLV_MEL_PAP_1 | 274 | 280 | PF00089 | 0.278 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.231 |
DEG_APCC_DBOX_1 | 531 | 539 | PF00400 | 0.431 |
DEG_SCF_TRCP1_1 | 453 | 458 | PF00400 | 0.431 |
DOC_CDC14_PxL_1 | 2 | 10 | PF14671 | 0.446 |
DOC_CKS1_1 | 207 | 212 | PF01111 | 0.474 |
DOC_CKS1_1 | 630 | 635 | PF01111 | 0.431 |
DOC_CKS1_1 | 703 | 708 | PF01111 | 0.523 |
DOC_MAPK_gen_1 | 224 | 234 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 26 | 35 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 589 | 598 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 589 | 598 | PF00069 | 0.351 |
DOC_PP1_RVXF_1 | 142 | 148 | PF00149 | 0.431 |
DOC_PP1_RVXF_1 | 696 | 702 | PF00149 | 0.478 |
DOC_PP2B_PxIxI_1 | 593 | 599 | PF00149 | 0.325 |
DOC_PP4_FxxP_1 | 630 | 633 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.434 |
DOC_USP7_UBL2_3 | 22 | 26 | PF12436 | 0.405 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 201 | 205 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 277 | 281 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 552 | 568 | PF00022 | 0.332 |
LIG_AP2alpha_2 | 396 | 398 | PF02296 | 0.431 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_2 | 91 | 97 | PF00533 | 0.474 |
LIG_EVH1_1 | 206 | 210 | PF00568 | 0.474 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.447 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.447 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.431 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.455 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.431 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.436 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.431 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.431 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.431 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.431 |
LIG_FHA_2 | 532 | 538 | PF00498 | 0.431 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.431 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.431 |
LIG_GBD_Chelix_1 | 250 | 258 | PF00786 | 0.231 |
LIG_LIR_Apic_2 | 203 | 207 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 687 | 697 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 543 | 549 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 687 | 692 | PF02991 | 0.433 |
LIG_MLH1_MIPbox_1 | 278 | 282 | PF16413 | 0.431 |
LIG_PCNA_yPIPBox_3 | 185 | 199 | PF02747 | 0.431 |
LIG_PCNA_yPIPBox_3 | 548 | 560 | PF02747 | 0.326 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.431 |
LIG_Pex14_2 | 278 | 282 | PF04695 | 0.478 |
LIG_Rb_LxCxE_1 | 256 | 273 | PF01857 | 0.457 |
LIG_SH2_CRK | 689 | 693 | PF00017 | 0.446 |
LIG_SH2_GRB2like | 465 | 468 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 560 | 563 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 465 | 468 | PF00017 | 0.474 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 622 | 626 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 237 | 240 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.431 |
LIG_SH3_1 | 204 | 210 | PF00018 | 0.431 |
LIG_SH3_1 | 309 | 315 | PF00018 | 0.446 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.431 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.446 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.431 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.431 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.438 |
LIG_SH3_3 | 680 | 686 | PF00018 | 0.431 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.345 |
LIG_SH3_5 | 685 | 689 | PF00018 | 0.431 |
LIG_SUMO_SIM_par_1 | 31 | 37 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 712 | 719 | PF11976 | 0.407 |
LIG_SxIP_EBH_1 | 700 | 709 | PF03271 | 0.431 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.431 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.474 |
LIG_TRAF2_1 | 632 | 635 | PF00917 | 0.474 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.431 |
LIG_UBA3_1 | 146 | 154 | PF00899 | 0.431 |
LIG_UBA3_1 | 660 | 669 | PF00899 | 0.474 |
LIG_UBA3_1 | 714 | 723 | PF00899 | 0.432 |
MOD_CDK_SPxxK_3 | 206 | 213 | PF00069 | 0.474 |
MOD_CDK_SPxxK_3 | 702 | 709 | PF00069 | 0.525 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.431 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.431 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.436 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.431 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.431 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.431 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.431 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.431 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.431 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.431 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.433 |
MOD_Cter_Amidation | 590 | 593 | PF01082 | 0.371 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.231 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.231 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.231 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.274 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.250 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.207 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.274 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.501 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.431 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.431 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.428 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.431 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.431 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.431 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.431 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.403 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.431 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.431 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.468 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.367 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.435 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.431 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.431 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.431 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.431 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.431 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.466 |
MOD_PK_1 | 228 | 234 | PF00069 | 0.390 |
MOD_PKA_1 | 413 | 419 | PF00069 | 0.478 |
MOD_PKA_1 | 508 | 514 | PF00069 | 0.474 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.447 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.457 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.394 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.431 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.431 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.431 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.431 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.474 |
MOD_Plk_2-3 | 688 | 694 | PF00069 | 0.446 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.431 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.455 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.399 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.456 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.412 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.431 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.431 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.460 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.446 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.474 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.431 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.431 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 138 | 146 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 37 | 46 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 474 | 483 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_1 | 141 | 146 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 689 | 692 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 592 | 595 | PF00400 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.231 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 658 | 663 | PF00026 | 0.231 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P664 | Leptomonas seymouri | 86% | 99% |
A0A0S4ISJ2 | Bodo saltans | 74% | 100% |
A0A3S7X0D3 | Leishmania donovani | 97% | 100% |
A4HFE8 | Leishmania braziliensis | 91% | 100% |
A4I2L1 | Leishmania infantum | 97% | 100% |
A7IQE5 | Xanthobacter autotrophicus (strain ATCC BAA-1158 / Py2) | 33% | 100% |
E9AYT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
I3VE77 | Aquincola tertiaricarbonis | 41% | 100% |
O86028 | Rhizobium meliloti (strain 1021) | 58% | 100% |
P11653 | Propionibacterium freudenreichii subsp. shermanii | 58% | 99% |
P16332 | Mus musculus | 63% | 97% |
P22033 | Homo sapiens | 63% | 96% |
P27253 | Escherichia coli (strain K12) | 59% | 100% |
P65488 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 56% | 96% |
P9WJK4 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 56% | 96% |
P9WJK5 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 56% | 96% |
Q05065 | Streptomyces virginiae | 58% | 99% |
Q1LRY0 | Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) | 35% | 66% |
Q23381 | Caenorhabditis elegans | 64% | 97% |
Q3IZ90 | Cereibacter sphaeroides (strain ATCC 17023 / DSM 158 / JCM 6121 / CCUG 31486 / LMG 2827 / NBRC 12203 / NCIMB 8253 / ATH 2.4.1.) | 32% | 100% |
Q3J4D7 | Cereibacter sphaeroides (strain ATCC 17023 / DSM 158 / JCM 6121 / CCUG 31486 / LMG 2827 / NBRC 12203 / NCIMB 8253 / ATH 2.4.1.) | 62% | 100% |
Q49115 | Methylorubrum extorquens (strain ATCC 14718 / DSM 1338 / JCM 2805 / NCIMB 9133 / AM1) | 33% | 100% |
Q59676 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 26% | 100% |
Q59677 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 61% | 100% |
Q5KUG0 | Geobacillus kaustophilus (strain HTA426) | 34% | 67% |
Q5RFN2 | Pongo abelii | 63% | 96% |
Q5Z110 | Nocardia farcinica (strain IFM 10152) | 34% | 68% |
Q8HXX1 | Macaca fascicularis | 63% | 96% |
Q8MI68 | Sus scrofa | 63% | 96% |
Q9GK13 | Bos taurus | 63% | 96% |