GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Chlorobium phaeobacteroides BS1

Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_012475142.1 CPHAMN1_RS08710 homocitrate synthase

Query= BRENDA::P58637
         (376 letters)



>NCBI__GCF_000020545.1:WP_012475142.1
          Length = 383

 Score =  257 bits (657), Expect = 3e-73
 Identities = 149/362 (41%), Positives = 213/362 (58%), Gaps = 2/362 (0%)

Query: 6   INDTTLRDGEQAAGVAFSVEEKIAIAKFLDAIGVHEIEVGIPAMGKAEQEAIANIVKLDL 65
           I DTTLRDGEQA GV FS EEK  IA  +  IG  E+E+G PA+   EQ  I  IV + L
Sbjct: 9   IIDTTLRDGEQAPGVVFSPEEKKDIAAMIADIGADELEIGYPAISVDEQRVIREIVAMKL 68

Query: 66  SANLLGWNRAVIADIQASIACGLQRVHISIPVSAIQIAVKFHGQWQVVLQKLHDSISFAV 125
              L  W+RA  +DI+ +  C  + +HIS P+S + + +     +  V ++L   I  A 
Sbjct: 69  PKRLTCWSRAKRSDIECASRCETEGIHISFPISNLYLDL-MGKDYLWVREQLEILIPEAK 127

Query: 126 DQGLFVSIGGEDSSRAEESFLLDVVLAAQEWGASRFRFCDTVGILDPFTTHAKVKQLVAS 185
               FVS G +D++R + + L      A   GA R R  DTVGI  P T    ++QL +S
Sbjct: 128 KHFSFVSAGAQDATRTDVTTLEAFARDASLCGADRVRIADTVGIATPLTLMRHIEQLKSS 187

Query: 186 LTIPVEMHTHNDFGLATANALAGTKAGALSVNTTVNGLGERAGNAALEEVVMALKHLYHH 245
           +TIP+E H HND G+ATANA +  +AG  +V+ +VNGLGERAGNAALEE+ +ALK    +
Sbjct: 188 VTIPLEFHAHNDLGMATANAFSAIEAGCDAVSVSVNGLGERAGNAALEELSLALKLSGRY 247

Query: 246 DLGIDTRRLLEISQLVASASGHPVPPWKAIVGENTFAHESGIHAHGVLQNPQTYEPFAPE 305
              I T RL  + + VA AS   +   K + G   F HESGIH + +L++P +Y+PF P 
Sbjct: 248 RNSIKTDRLHRLCEKVAKASNRIIQDQKPVTGSAVFQHESGIHCNALLKDPLSYQPFLPG 307

Query: 306 EVGRER-RLVVGKHSGRHLLSSILQQHDIILNHEETQFVLDAVRQESVEKKRSLTDQELL 364
           ++G+E   LV+GKHSG   +   ++ + I ++ EE   +L +VR  +  KK  L+  EL+
Sbjct: 308 DIGKEAYELVIGKHSGSASIQHAMEANGISIDREEAGKMLLSVRLAANRKKSGLSSAELM 367

Query: 365 HL 366
           ++
Sbjct: 368 NI 369


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: 341
Number of extensions: 16
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: 376
Length of database: 383
Length adjustment: 30
Effective length of query: 346
Effective length of database: 353
Effective search space:   122138
Effective search space used:   122138
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.

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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