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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H615
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009249 | protein lipoylation | 5 | 10 |
GO:0018193 | peptidyl-amino acid modification | 5 | 10 |
GO:0018205 | peptidyl-lysine modification | 6 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0051604 | protein maturation | 4 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016746 | acyltransferase activity | 3 | 1 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 1 |
GO:0017118 | lipoyltransferase activity | 5 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016979 | lipoate-protein ligase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.210 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.250 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.210 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.250 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.378 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.334 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.634 |
DEG_SPOP_SBC_1 | 419 | 423 | PF00917 | 0.572 |
DOC_ANK_TNKS_1 | 97 | 104 | PF00023 | 0.483 |
DOC_CYCLIN_RxL_1 | 495 | 502 | PF00134 | 0.416 |
DOC_CYCLIN_RxL_1 | 59 | 68 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.464 |
DOC_MIT_MIM_1 | 349 | 357 | PF04212 | 0.402 |
DOC_PP1_RVXF_1 | 69 | 76 | PF00149 | 0.346 |
DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.343 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.501 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 274 | 278 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 325 | 332 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 409 | 415 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 442 | 449 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.464 |
LIG_APCC_ABBAyCdc20_2 | 163 | 169 | PF00400 | 0.433 |
LIG_Clathr_ClatBox_1 | 289 | 293 | PF01394 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 331 | 339 | PF00928 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 502 | 510 | PF00928 | 0.418 |
LIG_eIF4E_1 | 186 | 192 | PF01652 | 0.528 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.488 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.452 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.390 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.554 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.398 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.388 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.465 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.341 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.473 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.264 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.463 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.479 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.525 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.540 |
LIG_Integrin_RGD_1 | 314 | 316 | PF01839 | 0.481 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 331 | 337 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 358 | 366 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 49 | 56 | PF02991 | 0.361 |
LIG_LIR_LC3C_4 | 38 | 42 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.363 |
LIG_NRBOX | 443 | 449 | PF00104 | 0.452 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.460 |
LIG_SH2_GRB2like | 76 | 79 | PF00017 | 0.305 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.323 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.401 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.464 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.551 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.340 |
LIG_SH3_5 | 206 | 210 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 371 | 379 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 189 | 196 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.506 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.396 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.285 |
LIG_TRFH_1 | 9 | 13 | PF08558 | 0.535 |
LIG_UBA3_1 | 60 | 69 | PF00899 | 0.365 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.403 |
LIG_WRC_WIRS_1 | 336 | 341 | PF05994 | 0.320 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.435 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.382 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.403 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.416 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.255 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.438 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.552 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.344 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.303 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.422 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.455 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.382 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.403 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.478 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.456 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.433 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.320 |
MOD_Cter_Amidation | 308 | 311 | PF01082 | 0.477 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.242 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.233 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.444 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.542 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.516 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.733 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.683 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.304 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.575 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.530 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.413 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.438 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.447 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.408 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.603 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.372 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.562 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.445 |
MOD_N-GLC_2 | 122 | 124 | PF02516 | 0.264 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.595 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.475 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.463 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.428 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.568 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.433 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.404 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.460 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.476 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.389 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.497 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.390 |
MOD_PK_1 | 355 | 361 | PF00069 | 0.354 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.440 |
MOD_PKA_1 | 171 | 177 | PF00069 | 0.459 |
MOD_PKA_1 | 310 | 316 | PF00069 | 0.493 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.437 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.456 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.566 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.390 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.485 |
MOD_PKB_1 | 351 | 359 | PF00069 | 0.360 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.502 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.311 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.510 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.342 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.516 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.522 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.673 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.406 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.467 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.378 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.494 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.441 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.402 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.407 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.406 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.365 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.491 |
TRG_NES_CRM1_1 | 349 | 362 | PF08389 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 202 | 207 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 62 | 67 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I310 | Leptomonas seymouri | 58% | 100% |
A0A0S4IZJ4 | Bodo saltans | 34% | 82% |
A0A1X0NQ94 | Trypanosomatidae | 39% | 100% |
A0A3R7MGW3 | Trypanosoma rangeli | 40% | 99% |
A4H555 | Leishmania braziliensis | 78% | 100% |
C9ZUI2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ALC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QII0 | Leishmania major | 91% | 100% |