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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
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: Q9U112
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 6 |
GO:0006518 | peptide metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009059 | macromolecule biosynthetic process | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018206 | peptidyl-methionine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 6 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043603 | amide metabolic process | 3 | 6 |
GO:0043604 | amide biosynthetic process | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
GO:0006508 | proteolysis | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 6 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 6 |
GO:0042586 | peptide deformylase activity | 5 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008237 | metallopeptidase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.497 |
CLV_PCSK_PC7_1 | 35 | 41 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 362 | 370 | PF00400 | 0.274 |
DEG_APCC_DBOX_1 | 452 | 460 | PF00400 | 0.551 |
DOC_ANK_TNKS_1 | 200 | 207 | PF00023 | 0.477 |
DOC_CKS1_1 | 416 | 421 | PF01111 | 0.344 |
DOC_CYCLIN_RxL_1 | 35 | 48 | PF00134 | 0.491 |
DOC_CYCLIN_RxL_1 | 89 | 97 | PF00134 | 0.480 |
DOC_MAPK_DCC_7 | 39 | 49 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 35 | 46 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 359 | 366 | PF00069 | 0.274 |
DOC_MAPK_gen_1 | 90 | 98 | PF00069 | 0.672 |
DOC_MAPK_MEF2A_6 | 39 | 46 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 90 | 98 | PF00069 | 0.672 |
DOC_MAPK_NFAT4_5 | 39 | 47 | PF00069 | 0.486 |
DOC_MAPK_NFAT4_5 | 91 | 99 | PF00069 | 0.648 |
DOC_MAPK_RevD_3 | 364 | 380 | PF00069 | 0.274 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.478 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.469 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.655 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.274 |
DOC_PP4_FxxP_1 | 417 | 420 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.541 |
DOC_USP7_UBL2_3 | 469 | 473 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 101 | 108 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 117 | 125 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 153 | 162 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.234 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.348 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.547 |
LIG_BIR_III_2 | 426 | 430 | PF00653 | 0.425 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.274 |
LIG_EVH1_2 | 419 | 423 | PF00568 | 0.381 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.401 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.321 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.274 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.482 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.274 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.416 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.420 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.597 |
LIG_Integrin_RGD_1 | 483 | 485 | PF01839 | 0.588 |
LIG_LIR_Apic_2 | 277 | 282 | PF02991 | 0.347 |
LIG_LIR_Apic_2 | 415 | 420 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 391 | 398 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.673 |
LIG_LYPXL_yS_3 | 213 | 216 | PF13949 | 0.356 |
LIG_LYPXL_yS_3 | 256 | 259 | PF13949 | 0.274 |
LIG_LYPXL_yS_3 | 403 | 406 | PF13949 | 0.360 |
LIG_Pex14_1 | 224 | 228 | PF04695 | 0.274 |
LIG_Pex14_1 | 399 | 403 | PF04695 | 0.396 |
LIG_PTB_Apo_2 | 273 | 280 | PF02174 | 0.268 |
LIG_Rb_pABgroove_1 | 268 | 276 | PF01858 | 0.274 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.372 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.214 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.379 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.476 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.635 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.478 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.561 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.491 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.499 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.523 |
LIG_SUMO_SIM_par_1 | 353 | 358 | PF11976 | 0.345 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.440 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.299 |
LIG_TRAF2_1 | 458 | 461 | PF00917 | 0.440 |
LIG_UBA3_1 | 46 | 53 | PF00899 | 0.481 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.519 |
LIG_WW_3 | 12 | 16 | PF00397 | 0.478 |
MOD_CDC14_SPxK_1 | 12 | 15 | PF00782 | 0.474 |
MOD_CDK_SPK_2 | 130 | 135 | PF00069 | 0.557 |
MOD_CDK_SPxK_1 | 9 | 15 | PF00069 | 0.482 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.580 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.563 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.517 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.426 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.527 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.397 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.564 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.531 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.569 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.552 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.546 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.274 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.274 |
MOD_GlcNHglycan | 491 | 497 | PF01048 | 0.590 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.612 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.531 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.560 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.516 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.347 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.336 |
MOD_LATS_1 | 349 | 355 | PF00433 | 0.299 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.524 |
MOD_N-GLC_2 | 128 | 130 | PF02516 | 0.584 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.536 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.567 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.469 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.274 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.359 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.526 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.274 |
MOD_PK_1 | 164 | 170 | PF00069 | 0.536 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.560 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.589 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.492 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.340 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.309 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.406 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.713 |
MOD_Plk_2-3 | 402 | 408 | PF00069 | 0.364 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.347 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.434 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.340 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.610 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.498 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.389 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.472 |
MOD_SUMO_rev_2 | 300 | 309 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 430 | 438 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.274 |
TRG_DiLeu_BaLyEn_6 | 42 | 47 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.635 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.180 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 310 | 315 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 344 | 348 | PF00026 | 0.268 |
TRG_Pf-PMV_PEXEL_1 | 52 | 56 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P349 | Leptomonas seymouri | 66% | 100% |
A0A3S7WNT3 | Leishmania donovani | 92% | 100% |
A4HS79 | Leishmania infantum | 92% | 100% |
E9AK65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |