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: 25 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HIN8
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 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 | 281 | 285 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 377 | 381 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.368 |
CLV_PCSK_FUR_1 | 122 | 126 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.292 |
DEG_APCC_DBOX_1 | 218 | 226 | PF00400 | 0.568 |
DOC_CKS1_1 | 168 | 173 | PF01111 | 0.568 |
DOC_CYCLIN_RxL_1 | 182 | 192 | PF00134 | 0.568 |
DOC_MAPK_gen_1 | 406 | 415 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 85 | 94 | PF00069 | 0.610 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.465 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.520 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.520 |
DOC_USP7_MATH_2 | 30 | 36 | PF00917 | 0.520 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 124 | 134 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 201 | 210 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 409 | 416 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 139 | 157 | PF00022 | 0.565 |
LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.534 |
LIG_APCC_ABBA_1 | 477 | 482 | PF00400 | 0.568 |
LIG_CaM_IQ_9 | 139 | 155 | PF13499 | 0.568 |
LIG_Clathr_ClatBox_1 | 500 | 504 | PF01394 | 0.644 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.568 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.486 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.540 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.483 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.557 |
LIG_LIR_Apic_2 | 15 | 19 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 7 | 12 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 467 | 477 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 312 | 316 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.550 |
LIG_PTB_Apo_2 | 8 | 15 | PF02174 | 0.490 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.585 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 9 | 12 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 453 | 457 | PF00017 | 0.568 |
LIG_SH2_PTP2 | 9 | 12 | PF00017 | 0.568 |
LIG_SH2_SRC | 346 | 349 | PF00017 | 0.532 |
LIG_SH2_SRC | 9 | 12 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.542 |
LIG_SH3_4 | 493 | 500 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 226 | 234 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 411 | 418 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 498 | 509 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 220 | 228 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 446 | 452 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 498 | 514 | PF11976 | 0.641 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.562 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.568 |
LIG_TYR_ITIM | 248 | 253 | PF00017 | 0.568 |
LIG_WW_1 | 171 | 174 | PF00397 | 0.508 |
MOD_CDK_SPxK_1 | 339 | 345 | PF00069 | 0.572 |
MOD_CDK_SPxxK_3 | 318 | 325 | PF00069 | 0.577 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.568 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.566 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.550 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.551 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.532 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.565 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.518 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.552 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.568 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.568 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.594 |
MOD_Cter_Amidation | 108 | 111 | PF01082 | 0.392 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.343 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.589 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.545 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.545 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.588 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.327 |
MOD_N-GLC_2 | 403 | 405 | PF02516 | 0.368 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.486 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.580 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.528 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.470 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.519 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.570 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.504 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.574 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.552 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.493 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.434 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.561 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.499 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.568 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.618 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.749 |
MOD_Plk_2-3 | 56 | 62 | PF00069 | 0.567 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.547 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.532 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.373 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.524 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.597 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.568 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.585 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.545 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.575 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.535 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 414 | 422 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 428 | 433 | PF00179 | 0.537 |
TRG_DiLeu_BaEn_1 | 228 | 233 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_2 | 194 | 200 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_4 | 20 | 26 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.497 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 185 | 190 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 201 | 206 | PF00026 | 0.173 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDH4 | Leptomonas seymouri | 79% | 99% |
A0A0S4IWX5 | Bodo saltans | 31% | 88% |
A0A1X0P1D0 | Trypanosomatidae | 38% | 100% |
A0A3R7P1P7 | Trypanosoma rangeli | 38% | 100% |
A0A3S7X3V2 | Leishmania donovani | 94% | 100% |
A1DI25 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 23% | 91% |
A4I5Y5 | Leishmania infantum | 94% | 100% |
A4RFH6 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 92% |
A7SMR1 | Nematostella vectensis | 26% | 94% |
B0X6P7 | Culex quinquefasciatus | 24% | 87% |
B0XU47 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 24% | 91% |
B3LY71 | Drosophila ananassae | 23% | 94% |
B3LZN3 | Drosophila ananassae | 24% | 97% |
B3P1F9 | Drosophila erecta | 25% | 96% |
B3P8G6 | Drosophila erecta | 23% | 95% |
B4GFS1 | Drosophila persimilis | 25% | 97% |
B4GP93 | Drosophila persimilis | 22% | 98% |
B4HFV9 | Drosophila sechellia | 23% | 95% |
B4HHG8 | Drosophila sechellia | 24% | 96% |
B4JTN0 | Drosophila grimshawi | 23% | 94% |
B4JUM0 | Drosophila grimshawi | 22% | 95% |
B4K892 | Drosophila mojavensis | 23% | 94% |
B4KDI2 | Drosophila mojavensis | 23% | 96% |
B4LYI3 | Drosophila virilis | 23% | 94% |
B4M5A7 | Drosophila virilis | 23% | 96% |
B4N8Z4 | Drosophila willistoni | 24% | 96% |
B4NLG2 | Drosophila willistoni | 23% | 94% |
B4PNN4 | Drosophila yakuba | 25% | 96% |
B4PNV2 | Drosophila yakuba | 23% | 95% |
B4QT07 | Drosophila simulans | 24% | 96% |
B4R222 | Drosophila simulans | 23% | 95% |
B5DY99 | Drosophila pseudoobscura pseudoobscura | 22% | 94% |
C9ZRB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 95% |
E9B178 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
K7IM66 | Nasonia vitripennis | 25% | 95% |
O15371 | Homo sapiens | 24% | 97% |
O70194 | Mus musculus | 24% | 97% |
P0CN48 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 23% | 97% |
P0CN49 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 23% | 97% |
P30642 | Caenorhabditis elegans | 23% | 93% |
Q0ZB77 | Bombyx mori | 24% | 97% |
Q16UF8 | Aedes aegypti | 24% | 86% |
Q295S1 | Drosophila pseudoobscura pseudoobscura | 25% | 97% |
Q3T122 | Bos taurus | 24% | 97% |
Q4Q6Y6 | Leishmania major | 94% | 100% |
Q4R8R4 | Macaca fascicularis | 24% | 97% |
Q4X054 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 91% |
Q554U9 | Dictyostelium discoideum | 24% | 100% |
Q5AVZ0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 90% |
Q5R925 | Pongo abelii | 24% | 97% |
Q6AYK8 | Rattus norvegicus | 24% | 97% |
Q6P8G0 | Xenopus tropicalis | 25% | 96% |
Q7QBW3 | Anopheles gambiae | 24% | 91% |
Q9VCK0 | Drosophila melanogaster | 23% | 95% |
Q9VGC7 | Drosophila melanogaster | 24% | 96% |
V5B793 | Trypanosoma cruzi | 37% | 100% |