Align NAD(+)-dependent homoserine dehydrogenase; NAD(+)-dependent HSD; NgHSD; EC 1.1.1.3 (characterized)
to candidate WP_028489059.1 Q394_RS0109355 homoserine dehydrogenase
Query= SwissProt::Q5F8J4 (435 letters) >NCBI__GCF_000621325.1:WP_028489059.1 Length = 436 Score = 497 bits (1279), Expect = e-145 Identities = 257/437 (58%), Positives = 327/437 (74%), Gaps = 6/437 (1%) Query: 1 MKPVNIGLLGLGTVGGGAAAVLRDNAEEISRRLGREIRISAMCDLSEEKARQI-CPSAAF 59 M PV +GLLGLGTVGGG A VL+ NAEEI+RR GR I I +L +A ++ S Sbjct: 1 MDPVKVGLLGLGTVGGGTAIVLKRNAEEIARRAGRGIVIDYAANLDLSRAEELGLGSVRL 60 Query: 60 VKDPFELVARKDVDVVVELFGGTGIAKEAVLKAIENGKHIVTANKKLLAEYGNEIFPLAE 119 +D FE+V D+ +VVEL GG +A++ VL+AI NGKH+VTANK L+A +GNEIF A+ Sbjct: 61 TQDAFEVVNDPDIQIVVELIGGYTVARDLVLQAIRNGKHVVTANKALIALHGNEIFAAAQ 120 Query: 120 KQNVIVQFEAAVAGGIPIIKALREGLAANRIKSIAGIINGTSNFILSEMREKGSAFADVL 179 +Q V+V FEAAVAGGIP+IKA+REGLAANRI+ +AGIINGT NFIL+EMR+KG AFADVL Sbjct: 121 EQGVVVAFEAAVAGGIPVIKAVREGLAANRIEWLAGIINGTGNFILTEMRDKGRAFADVL 180 Query: 180 KEAQALGYAEADPTFDIEGNDAGHKITIMSALAFGTPMNFSACYLEGISKLDSRDIKYAE 239 EAQALGYAEADPTFD+EG DAGHK+TI+S++AFG P+ F Y EGI+K+ + D+ YA Sbjct: 181 AEAQALGYAEADPTFDVEGIDAGHKLTILSSIAFGIPLQFKQTYTEGITKITAEDVTYAT 240 Query: 240 ELGYRIKLLGVTRKTGKGIELRVHPTLIPESRLLANVDGVMNAVRVNADMVGETLYYGAG 299 ELGYRIK LG+ R+T KGIE RVHPTLIP RL+ANVDGVMNAV V D VG TLYYGAG Sbjct: 241 ELGYRIKHLGIARRTPKGIEQRVHPTLIPHRRLIANVDGVMNAVLVQGDAVGPTLYYGAG 300 Query: 300 AGALPTASAVVADIIDIARLVEADTAHRVPHLAFQPAQVQAQTILPMDEITSSYYLRVQA 359 AGA PTASAV+AD++D+ R + AD +RVPHLAFQ Q+ ILP++E+ +++YLR+ A Sbjct: 301 AGAEPTASAVIADLVDVTRALTADPENRVPHLAFQSGQLADTVILPIEEVETAFYLRMCA 360 Query: 360 KDEPGTLGQIAALLAQENVSIEALIQK---GVIDQTTAEIVILTHSTVEKHIKSAIAAIE 416 D PG L + +L ++SIEA IQK +D+ +I++LT E ++ AIAAIE Sbjct: 361 LDRPGVLADVTRILGDRHISIEAFIQKEPSSGVDK--VDIIMLTQRVREGNMNEAIAAIE 418 Query: 417 ALDCVEKPITMIRMESL 433 AL+ + +T IR+E+L Sbjct: 419 ALEAICSSVTRIRVETL 435 Lambda K H 0.318 0.135 0.369 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 530 Number of extensions: 12 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 435 Length of database: 436 Length adjustment: 32 Effective length of query: 403 Effective length of database: 404 Effective search space: 162812 Effective search space used: 162812 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory