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. | yes | yes: 5 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q3Q4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006351 | DNA-templated transcription | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009059 | macromolecule biosynthetic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 12 |
GO:0032774 | RNA biosynthetic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0097659 | nucleic acid-templated transcription | 6 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003746 | translation elongation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.652 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.451 |
CLV_PCSK_PC7_1 | 128 | 134 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.552 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.455 |
DEG_SCF_SKP2-CKS1_1 | 383 | 390 | PF00560 | 0.601 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.687 |
DOC_MAPK_gen_1 | 359 | 369 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 362 | 369 | PF00069 | 0.589 |
DOC_MAPK_NFAT4_5 | 362 | 370 | PF00069 | 0.614 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.783 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.579 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 441 | 446 | PF00244 | 0.427 |
LIG_APCC_ABBA_1 | 10 | 15 | PF00400 | 0.560 |
LIG_APCC_ABBAyCdc20_2 | 9 | 15 | PF00400 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.575 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.569 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.596 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.363 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.579 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.635 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.523 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.569 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.531 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.471 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.175 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.612 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.379 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 322 | 331 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.441 |
LIG_MYND_1 | 218 | 222 | PF01753 | 0.586 |
LIG_PCNA_PIPBox_1 | 426 | 435 | PF02747 | 0.531 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.603 |
LIG_SH2_GRB2like | 324 | 327 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 324 | 328 | PF00017 | 0.603 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.611 |
LIG_SH2_SRC | 324 | 327 | PF00017 | 0.613 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 446 | 449 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.437 |
LIG_SH3_1 | 273 | 279 | PF00018 | 0.609 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.598 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.771 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.785 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.651 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.584 |
LIG_TRAF2_1 | 406 | 409 | PF00917 | 0.609 |
LIG_TYR_ITSM | 320 | 327 | PF00017 | 0.636 |
LIG_UBA3_1 | 426 | 434 | PF00899 | 0.540 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.565 |
MOD_CDK_SPK_2 | 384 | 389 | PF00069 | 0.599 |
MOD_CDK_SPxK_1 | 384 | 390 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.787 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.590 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.613 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.730 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.716 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.612 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.591 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.492 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.554 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.374 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.344 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.556 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.379 |
MOD_Cter_Amidation | 438 | 441 | PF01082 | 0.444 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.627 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.694 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.710 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.707 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.548 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.711 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.726 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.696 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.810 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.525 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.395 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.600 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.708 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.704 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.573 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.730 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.716 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.544 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.628 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.485 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.502 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.394 |
MOD_N-GLC_1 | 427 | 432 | PF02516 | 0.533 |
MOD_N-GLC_2 | 64 | 66 | PF02516 | 0.597 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.453 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.744 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.609 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.565 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.511 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.622 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.669 |
MOD_PKA_1 | 350 | 356 | PF00069 | 0.394 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.586 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.394 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.512 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.582 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.601 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.509 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.493 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.643 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.604 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.595 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.451 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.367 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.609 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.700 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.760 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.668 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.617 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.567 |
MOD_SUMO_rev_2 | 201 | 207 | PF00179 | 0.578 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.618 |
TRG_DiLeu_BaEn_3 | 371 | 377 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.562 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 236 | 241 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 350 | 355 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZC4 | Leptomonas seymouri | 60% | 98% |
A0A0S4JM53 | Bodo saltans | 26% | 91% |
A0A0S4JM77 | Bodo saltans | 30% | 100% |
A0A1X0NRX7 | Trypanosomatidae | 39% | 99% |
A0A3Q8IGU5 | Leishmania donovani | 93% | 100% |
A0A3R7KDK8 | Trypanosoma rangeli | 38% | 100% |
A4HLZ2 | Leishmania braziliensis | 81% | 100% |
A4I9C2 | Leishmania infantum | 93% | 100% |
C9ZJ99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B4C1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
V5BJM3 | Trypanosoma cruzi | 36% | 99% |