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: 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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
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 |
GO:0005654 | nucleoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HLZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006351 | DNA-templated transcription | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0032774 | RNA biosynthetic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0097659 | nucleic acid-templated transcription | 6 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003746 | translation elongation factor activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.427 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.336 |
CLV_PCSK_PC7_1 | 128 | 134 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.464 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.355 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.519 |
DEG_SCF_SKP2-CKS1_1 | 384 | 391 | PF00560 | 0.502 |
DEG_SCF_TRCP1_1 | 312 | 318 | PF00400 | 0.431 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.587 |
DOC_ANK_TNKS_1 | 134 | 141 | PF00023 | 0.458 |
DOC_MAPK_gen_1 | 360 | 370 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 191 | 199 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 33 | 41 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 363 | 370 | PF00069 | 0.477 |
DOC_MAPK_NFAT4_5 | 363 | 371 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 250 | 257 | PF00149 | 0.380 |
DOC_PP1_RVXF_1 | 277 | 283 | PF00149 | 0.448 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.270 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 23 | 30 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 252 | 257 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 442 | 447 | PF00244 | 0.305 |
LIG_APCC_ABBA_1 | 10 | 15 | PF00400 | 0.485 |
LIG_APCC_ABBAyCdc20_2 | 9 | 15 | PF00400 | 0.483 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.614 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.508 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.258 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.510 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.541 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.429 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.437 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.388 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.121 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.525 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.322 |
LIG_LIR_Apic_2 | 281 | 285 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.357 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.403 |
LIG_SH2_GRB2like | 325 | 328 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.403 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.539 |
LIG_SH2_SRC | 325 | 328 | PF00017 | 0.544 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.399 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 392 | 395 | PF00017 | 0.499 |
LIG_SH2_STAT3 | 447 | 450 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.328 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.521 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.523 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.462 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.497 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.506 |
LIG_TYR_ITSM | 321 | 328 | PF00017 | 0.431 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.488 |
MOD_CDK_SPK_2 | 385 | 390 | PF00069 | 0.499 |
MOD_CDK_SPxK_1 | 385 | 391 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 269 | 276 | PF00069 | 0.695 |
MOD_CDK_SPxxK_3 | 315 | 322 | PF00069 | 0.406 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.500 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.555 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.593 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.576 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.445 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.548 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.501 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.501 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.403 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.461 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.252 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.235 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.464 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.323 |
MOD_Cter_Amidation | 439 | 442 | PF01082 | 0.326 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.633 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.672 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.475 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.593 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.586 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.587 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.700 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.394 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.268 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.470 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.562 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.576 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.616 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.505 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.505 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.577 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.542 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.343 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.361 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.275 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.404 |
MOD_N-GLC_2 | 64 | 66 | PF02516 | 0.426 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.345 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.594 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.438 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.436 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.424 |
MOD_NEK2_2 | 335 | 340 | PF00069 | 0.457 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.565 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.541 |
MOD_PK_1 | 191 | 197 | PF00069 | 0.428 |
MOD_PKA_1 | 171 | 177 | PF00069 | 0.279 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.525 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.566 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.394 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.387 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.509 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.368 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.378 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.505 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.394 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.261 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.165 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.511 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.573 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.646 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.588 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.442 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.406 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 201 | 207 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 213 | 223 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 362 | 367 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_3 | 372 | 378 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_4 | 164 | 170 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 236 | 241 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 351 | 356 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZC4 | Leptomonas seymouri | 59% | 99% |
A0A0S4JM53 | Bodo saltans | 25% | 91% |
A0A1X0NRX7 | Trypanosomatidae | 38% | 99% |
A0A3Q8IGU5 | Leishmania donovani | 82% | 100% |
A0A3R7KDK8 | Trypanosoma rangeli | 36% | 100% |
A4I9C2 | Leishmania infantum | 82% | 100% |
C9ZJ99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B4C1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q2KI09 | Bos taurus | 23% | 100% |
Q4Q3Q4 | Leishmania major | 81% | 99% |
V5BJM3 | Trypanosoma cruzi | 38% | 99% |