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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HMN6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.574 |
CLV_MEL_PAP_1 | 37 | 43 | PF00089 | 0.569 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.506 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.281 |
CLV_Separin_Metazoa | 474 | 478 | PF03568 | 0.517 |
DEG_APCC_DBOX_1 | 164 | 172 | PF00400 | 0.510 |
DOC_CKS1_1 | 197 | 202 | PF01111 | 0.499 |
DOC_CYCLIN_RxL_1 | 174 | 184 | PF00134 | 0.465 |
DOC_CYCLIN_yCln2_LP_2 | 385 | 391 | PF00134 | 0.361 |
DOC_MAPK_DCC_7 | 347 | 357 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 220 | 230 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 86 | 95 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 223 | 230 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 494 | 503 | PF00069 | 0.467 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.360 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.636 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 211 | 221 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 522 | 530 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.521 |
LIG_APCC_ABBA_1 | 171 | 176 | PF00400 | 0.330 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.463 |
LIG_BRCT_BRCA1_1 | 37 | 41 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.392 |
LIG_DLG_GKlike_1 | 191 | 198 | PF00625 | 0.542 |
LIG_eIF4E_1 | 174 | 180 | PF01652 | 0.346 |
LIG_eIF4E_1 | 28 | 34 | PF01652 | 0.445 |
LIG_eIF4E_1 | 483 | 489 | PF01652 | 0.448 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.360 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.367 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.306 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.413 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.434 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.526 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.421 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.480 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.635 |
LIG_LIR_Apic_2 | 194 | 200 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 514 | 525 | PF02991 | 0.535 |
LIG_LIR_LC3C_4 | 224 | 228 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.624 |
LIG_LRP6_Inhibitor_1 | 350 | 356 | PF00058 | 0.299 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.281 |
LIG_PCNA_yPIPBox_3 | 183 | 196 | PF02747 | 0.458 |
LIG_PCNA_yPIPBox_3 | 339 | 349 | PF02747 | 0.255 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.468 |
LIG_SH2_SRC | 505 | 508 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 234 | 237 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.372 |
LIG_SH3_2 | 296 | 301 | PF14604 | 0.362 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.426 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.360 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 176 | 182 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 382 | 387 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 382 | 387 | PF11976 | 0.498 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.675 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.663 |
LIG_TRAF2_2 | 200 | 205 | PF00917 | 0.280 |
LIG_UBA3_1 | 138 | 147 | PF00899 | 0.484 |
LIG_WRC_WIRS_1 | 138 | 143 | PF05994 | 0.524 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.532 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.367 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.690 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.739 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.492 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.530 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.440 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.449 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.405 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.728 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.702 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.463 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.433 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.642 |
MOD_Cter_Amidation | 66 | 69 | PF01082 | 0.476 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.428 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.513 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.405 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.558 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.493 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.615 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.564 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.726 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.305 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.595 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.509 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.459 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.481 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.366 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.264 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.432 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.691 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.497 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.570 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.724 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.485 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.600 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.419 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.451 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.621 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.478 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.454 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.381 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.357 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.413 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.418 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.497 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.369 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.362 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.403 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.497 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.590 |
MOD_PKA_1 | 521 | 527 | PF00069 | 0.663 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.526 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.291 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.366 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.610 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.545 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.478 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.370 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.558 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.553 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.442 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.494 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.534 |
MOD_Plk_2-3 | 464 | 470 | PF00069 | 0.621 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.357 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.484 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.550 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.391 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.351 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.318 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.150 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.508 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.325 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.496 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.646 |
MOD_SUMO_rev_2 | 140 | 149 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 402 | 411 | PF00179 | 0.596 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_2 | 372 | 378 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.310 |
TRG_NLS_MonoCore_2 | 67 | 72 | PF00514 | 0.577 |
TRG_NLS_MonoExtC_3 | 67 | 72 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 68 | 74 | PF00514 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 494 | 498 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 535 | 539 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9E6 | Leptomonas seymouri | 66% | 99% |
A0A1X0P5Q0 | Trypanosomatidae | 42% | 100% |
A0A3R7RFL4 | Trypanosoma rangeli | 47% | 100% |
A0A3S7X984 | Leishmania donovani | 87% | 100% |
C9ZZF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AF38 | Leishmania major | 85% | 100% |
E9AHV5 | Leishmania infantum | 87% | 100% |
E9B693 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BTI6 | Trypanosoma cruzi | 46% | 100% |