Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HLW4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 25 |
GO:0006807 | nitrogen compound metabolic process | 2 | 25 |
GO:0008152 | metabolic process | 1 | 25 |
GO:0019538 | protein metabolic process | 3 | 25 |
GO:0043170 | macromolecule metabolic process | 3 | 25 |
GO:0044238 | primary metabolic process | 2 | 25 |
GO:0071704 | organic substance metabolic process | 2 | 25 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 25 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 25 |
GO:0004180 | carboxypeptidase activity | 5 | 25 |
GO:0004181 | metallocarboxypeptidase activity | 6 | 25 |
GO:0008233 | peptidase activity | 3 | 25 |
GO:0008235 | metalloexopeptidase activity | 5 | 25 |
GO:0008237 | metallopeptidase activity | 4 | 25 |
GO:0008238 | exopeptidase activity | 4 | 25 |
GO:0016787 | hydrolase activity | 2 | 25 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 25 |
GO:0016853 | isomerase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.271 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.329 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.265 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.488 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.326 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 380 | 389 | PF00244 | 0.212 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.380 |
LIG_Actin_WH2_2 | 169 | 187 | PF00022 | 0.278 |
LIG_BIR_III_4 | 38 | 42 | PF00653 | 0.295 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.265 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.295 |
LIG_deltaCOP1_diTrp_1 | 405 | 413 | PF00928 | 0.341 |
LIG_eIF4E_1 | 469 | 475 | PF01652 | 0.459 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.415 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.493 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.296 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.443 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.405 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.313 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.333 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.329 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.344 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.232 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.341 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.404 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.204 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.453 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 49 | 60 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.238 |
LIG_PCNA_yPIPBox_3 | 330 | 339 | PF02747 | 0.229 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.352 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.265 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 344 | 347 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.265 |
LIG_SH2_STAT3 | 425 | 428 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.211 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.346 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.307 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.323 |
LIG_UBA3_1 | 183 | 190 | PF00899 | 0.295 |
LIG_UBA3_1 | 429 | 435 | PF00899 | 0.459 |
LIG_WRC_WIRS_1 | 410 | 415 | PF05994 | 0.204 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.497 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.254 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.218 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.232 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.267 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.298 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.303 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.204 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.438 |
MOD_Cter_Amidation | 100 | 103 | PF01082 | 0.265 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.331 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.300 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.451 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.374 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.487 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.374 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.204 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.455 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.336 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.445 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.418 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.265 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.451 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.257 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.399 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.348 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.295 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.395 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.371 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.331 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.411 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.211 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.372 |
MOD_Plk_2-3 | 450 | 456 | PF00069 | 0.204 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.401 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.445 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.347 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.351 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.339 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.326 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.320 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.327 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.361 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.270 |
MOD_SUMO_for_1 | 34 | 37 | PF00179 | 0.265 |
MOD_SUMO_rev_2 | 116 | 126 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 436 | 442 | PF00179 | 0.265 |
MOD_SUMO_rev_2 | 53 | 63 | PF00179 | 0.295 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.204 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.265 |
TRG_DiLeu_BaEn_4 | 139 | 145 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.341 |
TRG_ER_FFAT_2 | 49 | 59 | PF00635 | 0.204 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.227 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ28 | Bodo saltans | 44% | 100% |
A0A1X0NY67 | Trypanosomatidae | 52% | 98% |
A0A1X0P441 | Trypanosomatidae | 57% | 99% |
A0A1X0P598 | Trypanosomatidae | 58% | 99% |
A0A3Q8IBW2 | Leishmania donovani | 52% | 99% |
A0A3Q8IJY8 | Leishmania donovani | 46% | 100% |
A0A3Q8IU74 | Leishmania donovani | 86% | 100% |
A0A3S7WSA3 | Leishmania donovani | 55% | 99% |
A0A422P042 | Trypanosoma rangeli | 58% | 99% |
A0A422P4R1 | Trypanosoma rangeli | 53% | 99% |
A4H716 | Leishmania braziliensis | 54% | 100% |
A4HVE5 | Leishmania infantum | 55% | 99% |
A4HVW0 | Leishmania infantum | 52% | 99% |
A4I993 | Leishmania infantum | 85% | 100% |
A4IC85 | Leishmania infantum | 46% | 100% |
D0A656 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 99% |
E9AP43 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 99% |
E9B493 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
P42663 | Thermus aquaticus | 34% | 97% |
P50848 | Bacillus subtilis (strain 168) | 34% | 99% |
Q4Q0D4 | Leishmania major | 48% | 100% |
Q4Q3T3 | Leishmania major | 84% | 100% |
Q4QFW7 | Leishmania major | 52% | 100% |
Q4QGE5 | Leishmania major | 56% | 100% |
Q5SLM3 | Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) | 32% | 98% |
Q8U3L0 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 32% | 100% |
V5DQA0 | Trypanosoma cruzi | 60% | 99% |