GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tpiA in Methylobacterium nodulans ORS 2060

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_015933584.1 MNOD_RS34460 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000022085.1:WP_015933584.1
          Length = 398

 Score =  349 bits (896), Expect = e-100
 Identities = 182/386 (47%), Positives = 254/386 (65%), Gaps = 2/386 (0%)

Query: 10  DLKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPKGEPSP 69
           DLKGKRV++RVD NVP+++G V D TRI   LPTI+   E G +V+LL+H GRPKG+P P
Sbjct: 12  DLKGKRVLVRVDLNVPMENGRVTDATRITRVLPTIREIAEAGGRVVLLAHFGRPKGKPDP 71

Query: 70  EFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPE 129
           + SL P+A+ +++ LG+ V F    +G +  +AV  L +G V +LENTRFH GE KNDP 
Sbjct: 72  KESLRPIAEAVAKDLGRPVAFAEDCIGPKAAEAVAALGDGGVAMLENTRFHAGEEKNDPA 131

Query: 130 LAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIPSVAGFLMEKEIKFLSKVTYNPEKPY 189
             +  A+  D++VN+AF  +HRAHAS  G+A  +P+ AG LM+ EI+ L+K    P +P 
Sbjct: 132 FVQALAANGDVYVNEAFSASHRAHASTEGLAHVLPAYAGRLMQAEIEALTKGLEAPARPV 191

Query: 190 VVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKEL 249
           V ++GG+KVS KI ++ NL+ K D ++IGG M  TFL A G  VG S  E D    A  +
Sbjct: 192 VAIVGGSKVSTKIDLLVNLVGKVDALVIGGGMANTFLHATGLGVGRSLCERDLAGTALRI 251

Query: 250 LEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKLS 309
           +E A+EK   I+LPVDAV+A++ +         I D IPE  M LD+G +++E     L+
Sbjct: 252 IEAAREKNCAIILPVDAVVAEEFKANAPHHTYGI-DAIPESGMILDVGAQSVERVAAALN 310

Query: 310 DAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKG-AITVVGGGDSAAAVNKFGLEDK 368
           DAKT+VWNGP+G FE   F +GT   A   A  T+ G  ++V GGGD+ AA+N  G+ + 
Sbjct: 311 DAKTLVWNGPLGAFEFPPFDQGTVAAARHAAERTKAGKLVSVAGGGDTVAALNHAGVAEA 370

Query: 369 FSHVSTGGGASLEFLEGKELPGIASI 394
           F++VST GGA LE+LEGK LPG+ ++
Sbjct: 371 FTYVSTAGGAFLEWLEGKPLPGVDAL 396


Lambda     K      H
   0.317    0.137    0.386 

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: 613
Number of extensions: 27
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: 654
Length of database: 398
Length adjustment: 34
Effective length of query: 620
Effective length of database: 364
Effective search space:   225680
Effective search space used:   225680
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 (21.6 bits)
S2: 52 (24.6 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