GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Chlorobaculum tepidum TLS

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate NP_660976.1 CT0070 class V aminotransferase

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000006985.1:NP_660976.1
          Length = 379

 Score =  276 bits (706), Expect = 7e-79
 Identities = 157/378 (41%), Positives = 238/378 (62%), Gaps = 13/378 (3%)

Query: 4   KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSG 63
           K+ L  PGPTPVPE V+L MA   I HR+ +F +I+  +  NLK+L +T   V+++T SG
Sbjct: 2   KKRLFTPGPTPVPENVMLRMAAPIIHHRNPEFMEILERVHENLKYLFRTTQPVVVMTCSG 61

Query: 64  TGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTF-GLAVEEIKAEWGKALDPNDFKT 122
           TG MEA+I +    GD+++  N GKFG+RW ++A+ + G  VEE K EWG A+ P     
Sbjct: 62  TGGMEAAISSLFRQGDKLITINGGKFGERWSELARIYTGNCVEE-KIEWGTAISPERIAE 120

Query: 123 LLEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIVDAVTSLGATPVAIDD 182
           LL+   D     + ITHSETSTG  +D+ A+ AA +    AL++VD +T++GA     DD
Sbjct: 121 LLDEHPD--AMGVCITHSETSTGTASDVRALCAAIRERSEALILVDGITAIGAHEFHFDD 178

Query: 183 LGLDVVASGSQKGYMIPPGLGFVSVSAKAWQ-AYETATIPRFYLDLKKYKKSTDEDSSPF 241
            G D+  +GSQKG M+PPGL  V+VS +A +  +     P++YL L+K  KS   + +PF
Sbjct: 179 WGADICITGSQKGLMMPPGLALVAVSERAQEIIHNRKHQPQYYLSLRKALKSHAGNDTPF 238

Query: 242 TPPINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNAITA 301
           TP ++L+ GL  +LQM++AEG++ ++ RH+    A R   +AL + LF+   + S A+TA
Sbjct: 239 TPAVSLIIGLDEALQMLRAEGIENVWARHEALAGACRLGCQALGMELFS--ESPSYAVTA 296

Query: 302 V-APLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATL 360
           V  P G + ++  +T++ K  I +A GQD  KG+IFRI HLG+  + D+L+ +G LE +L
Sbjct: 297 VWLPEGADWKEFNTTLKIKNGITVAAGQDDFKGRIFRISHLGYYDELDMLTLMGGLERSL 356

Query: 361 --IELGYEGVTPGSGVAA 376
             +E+ +     G+GV+A
Sbjct: 357 KMMEIPFR---VGAGVSA 371


Lambda     K      H
   0.317    0.134    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: 321
Number of extensions: 10
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: 384
Length of database: 379
Length adjustment: 30
Effective length of query: 354
Effective length of database: 349
Effective search space:   123546
Effective search space used:   123546
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: 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