GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuA in Heliomicrobium modesticaldum Ice1; ATCC 51547

Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_012282226.1 HM1_RS05075 homocitrate synthase

Query= curated2:Q8RCF9
         (384 letters)



>NCBI__GCF_000019165.1:WP_012282226.1
          Length = 380

 Score =  327 bits (837), Expect = 4e-94
 Identities = 167/363 (46%), Positives = 233/363 (64%)

Query: 9   VYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKL 68
           V+++DTTLRDGEQT GV F   EK  +A+ L E G+ ++E G+P MG DE+ET+A+I KL
Sbjct: 5   VWLMDTTLRDGEQTPGVAFCPQEKALLARRLAEAGVHEIETGVPAMGEDEQETIARIVKL 64

Query: 69  GLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRF 128
            L   +  WNRAV+ D++ SL CGV +VAI + +SD  I  KL+++RQWVLD M   VR 
Sbjct: 65  NLPTRVTTWNRAVISDLEASLNCGVRSVAICLPSSDQQITQKLRQSRQWVLDQMGACVRR 124

Query: 129 AKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIK 188
           AK EG+YV +  EDASR D  FLI+    A++   +RLR  DT+G LDP +T+ +   + 
Sbjct: 125 AKAEGLYVVIGLEDASRADPQFLIQLGLEAERLKVNRLRISDTLGILDPIRTFNLFDRLT 184

Query: 189 DAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVY 248
            ++ I +E+H HND GMATAN ++ ++AGAK   VTV GLGERAGNA LEEV +AL+   
Sbjct: 185 SSLSIPLEIHAHNDLGMATANTVSAIQAGAKAASVTVCGLGERAGNAPLEEVALALRQCC 244

Query: 249 KMDLGIDTSRFREISEYVALASGRPLPPSKAIVGKNVFAHESGIHVDGALKNPYTYEVFD 308
             D  I+ +    +   V+ ++ RP+P SK +VG++ F H S IHVDG  K+   YE + 
Sbjct: 245 AADTRINLALLPALCRLVSWSTRRPIPFSKPVVGRDAFTHASSIHVDGLNKDRSNYEAYP 304

Query: 309 PQEVGLERQIVIGKHSGTAALINKFKEYGRVLTEEEANLLLPHVRKMAIQLKRPLFDKEL 368
           P+ VG   +I  GK+SG   L    K  G  L +EE   LL +VR+++  LKRPL   ++
Sbjct: 305 PEYVGRRHRIAFGKYSGRKLLAELLKAQGHDLDQEEMTQLLLNVRQLSQVLKRPLRQHDI 364

Query: 369 MYL 371
           + L
Sbjct: 365 VDL 367


Lambda     K      H
   0.318    0.135    0.379 

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: 322
Number of extensions: 6
Number of successful extensions: 1
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: 384
Length of database: 380
Length adjustment: 30
Effective length of query: 354
Effective length of database: 350
Effective search space:   123900
Effective search space used:   123900
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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