GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Desulfatibacillum aliphaticivorans DSM 15576

Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_028313261.1 G491_RS0101035 hypothetical protein

Query= BRENDA::P58637
         (376 letters)



>NCBI__GCF_000429905.1:WP_028313261.1
          Length = 374

 Score =  281 bits (720), Expect = 2e-80
 Identities = 165/369 (44%), Positives = 227/369 (61%), Gaps = 5/369 (1%)

Query: 4   VLINDTTLRDGEQAAGVAFSVEEKIAIAKFLDAIGVHEIEVGIPAMGKAEQEAIANIVKL 63
           V I DTTLRDGEQA G AF  +EKIA+A  LD   V E+E GIPAMG A Q+ I  I  L
Sbjct: 7   VHIIDTTLRDGEQAPGAAFDKKEKIALAIMLDQAHVDELEAGIPAMGAAAQDEIKAIAGL 66

Query: 64  DLSANLLGWNRAVIADIQASIACGLQRVHISIPVSAIQI-AVKFHGQWQVVLQKLHDSIS 122
           +L   L  W RA+  DI  S+ C +  VHIS PVS I + A+     W  VL +L + I 
Sbjct: 67  NLDCLLTAWCRALKDDIDQSLPCNVTGVHISFPVSDIHLDAMGKTSSW--VLDQLSELIP 124

Query: 123 FAVDQGLFVSIGGEDSSRAEESFLLDVVLAAQEWGASRFRFCDTVGILDPFTTHAKVKQL 182
           +A+ +   VS+G +D+ RA+ +FL   V +A   GA R R  DTVG+  P      V  L
Sbjct: 125 YALKRFSRVSVGAQDAFRADMAFLKQFVHSANLCGAHRVRIADTVGLARPSQVENMVHVL 184

Query: 183 V-ASLTIPVEMHTHNDFGLATANALAGTKAGALSVNTTVNGLGERAGNAALEEVVMALKH 241
             A+  + +E H HND G+ATAN +A  +AGA +V+ TVNGLGERAGNA LE+VV+A+  
Sbjct: 185 SRAAGKMALEFHGHNDLGMATANTIAAIEAGAQAVSVTVNGLGERAGNAPLEQVVVAVGT 244

Query: 242 LYHHDLGIDTRRLLEISQLVASASGHPVPPWKAIVGENTFAHESGIHAHGVLQNPQTYEP 301
           L      +D R + +I + VA A   P+P  + I G+  F HESGIH  G+L+NP TY+P
Sbjct: 245 LDSRSSCVDARHMNKICRYVAEAVNRPIPADQPITGQAVFTHESGIHCAGILKNPDTYQP 304

Query: 302 FAPEEVGRER-RLVVGKHSGRHLLSSILQQHDIILNHEETQFVLDAVRQESVEKKRSLTD 360
           F PE VGRER +LV+G+HSG  ++  +L +  + L   +T+ ++ AVR E+++K+  L+ 
Sbjct: 305 FNPETVGRERAQLVIGRHSGSGMVRHVLAKAGVRLEEGKTESLMAAVRMEALKKRSVLSP 364

Query: 361 QELLHLVQT 369
            EL+ +  T
Sbjct: 365 GELVRIYNT 373


Lambda     K      H
   0.319    0.133    0.383 

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: 343
Number of extensions: 17
Number of successful extensions: 4
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: 376
Length of database: 374
Length adjustment: 30
Effective length of query: 346
Effective length of database: 344
Effective search space:   119024
Effective search space used:   119024
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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