GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Clostridium acetobutylicum ATCC 824

Align phosphoserine aminotransferase monomer (EC 2.6.1.1; EC 2.6.1.52) (characterized)
to candidate NP_346661.1 CA_C0014 aminotransferase

Query= metacyc::MONOMER-15919
         (385 letters)



>NCBI__GCF_000008765.1:NP_346661.1
          Length = 356

 Score =  219 bits (558), Expect = 9e-62
 Identities = 139/341 (40%), Positives = 199/341 (58%), Gaps = 12/341 (3%)

Query: 8   KLLMIPGPTMVPPEVLNAMALPVIGHRTKDYSNLLEDTIEKLKKVFITENDTFLITGSGT 67
           K L IPGP  V  +VL  MA P+IGHR+K+ S+L     +KL+ VF T+ +  L T SG+
Sbjct: 3   KKLFIPGPVEVAEDVLQKMAEPMIGHRSKEASSLQRGISDKLRIVFQTKEEILLSTSSGS 62

Query: 68  AAMDMAISNIIKRGDKVLNIVTGNFGERFANIVKAYKGEAIRLDVEWGDMAEPEAVKEIL 127
             M+ AI     +   V +I  G FG+R+  +    +  A   +VEWG+  +PE V E+L
Sbjct: 63  GLMEGAIRCCTAKRAAVFSI--GAFGKRWYEMAIDNRVPADLYEVEWGEAIKPEFVDEVL 120

Query: 128 D--KYDDIKAVTVVHNETSTGARNPIKEIGEVVKDY-DALYIVDTVSSLGGDYVNVDKFH 184
              KYD    + + HNETSTG  NP+ EI +V+K Y + ++ +DTVSS+GG  + VD+  
Sbjct: 121 GTGKYD---LIALTHNETSTGIMNPVGEIAKVIKKYPEVVWCLDTVSSMGGTNIPVDELG 177

Query: 185 IDICVTGSQKCLAAPPGLAAITVSEKAWEVIKKNDDKVGFYLDLLAYKKYYEEKK-QTPY 243
           +D+C+T SQK L  PPGLAA + S+KA E  + N +  G+YLDLL   ++ ++K  Q P 
Sbjct: 178 VDVCITSSQKALGLPPGLAACSFSKKAIERAR-NVEHRGYYLDLLKLYEFIQKKDYQYPS 236

Query: 244 TPSVNLTYALNVALDLVLEEGIENRVKRHERLAKATRAGLEAMGIELFAKERARSVTVTS 303
           TPS++  +AL+ AL+ +LEEG++NR KRH  +A+  RA       E+F  E   S TVT+
Sbjct: 237 TPSLSHMFALDYALNKMLEEGMDNRYKRHIEMAEYVRAWAR-KNFEIFGDEDNLSNTVTT 295

Query: 304 AKYPEGIEDSKFRGILSNKYNIVVAGGQKHLAGKIFRIGHM 344
            K   GI  +     L  K    ++ G   L  K FRI HM
Sbjct: 296 IKNTRGISVADLNKEL-GKRGFAISNGYGKLKEKTFRIAHM 335


Lambda     K      H
   0.316    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: 371
Number of extensions: 14
Number of successful extensions: 6
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: 385
Length of database: 356
Length adjustment: 30
Effective length of query: 355
Effective length of database: 326
Effective search space:   115730
Effective search space used:   115730
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: 49 (23.5 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