GapMind for Amino acid biosynthesis

 

Alignments for a candidate for mesA in Methanothermobacter thermautotrophicus Delta H

Align Methionine synthase; Homocysteine methyltransferase; Methylcobalamin:homocysteine methyltransferase; EC 2.1.1.- (characterized)
to candidate WP_010876413.1 MTH_RS03635 methionine synthase

Query= SwissProt::P55299
         (309 letters)



>NCBI__GCF_000008645.1:WP_010876413.1
          Length = 308

 Score =  474 bits (1220), Expect = e-138
 Identities = 235/306 (76%), Positives = 266/306 (86%)

Query: 1   MITTVVGSYPATPREPETLRERISSFIGSYDACRPAIETAVRDQVRAGVDIISDGQVRGD 60
           MITTVVGSYP  PR PETL ER+ +F GSYD  RPAIE AVRDQ RAGVDIISDGQVRGD
Sbjct: 1   MITTVVGSYPTEPRGPETLGERLLNFFGSYDRYRPAIEAAVRDQFRAGVDIISDGQVRGD 60

Query: 61  MVGHFAEAMGGMMVKDGVSIIFSRITPPAGSIGSDDLIYAIKILRKLTDDESKGVKGIIT 120
           MVGHFA A+GGM ++DG SII+SRITPPAGSIG+ DL YA +ILR LTDDES+GVKGIIT
Sbjct: 61  MVGHFAAAIGGMKIEDGTSIIYSRITPPAGSIGAADLRYAYRILRGLTDDESRGVKGIIT 120

Query: 121 GPSTMAHASKIEGFYSPQKRERAIMDMADALRVEAEHLQDAGALMIQIDEPFLSTGMVDM 180
           GPSTM +AS+IEGFY PQKR+RA+MDMA  L++EA+HLQDAGA MIQIDEPFLSTG+VDM
Sbjct: 121 GPSTMIYASRIEGFYDPQKRDRAVMDMAGVLKIEAKHLQDAGAAMIQIDEPFLSTGIVDM 180

Query: 181 GTARRAVKRISGALDVDVSLHVCGDISGVIGELLTFPVDMLDLEFAGRPSNLEVLAEKWR 240
            TA RA+  I+  LD++VSLHVCGDI  V+ +LL F VD+LDLEFAGRPSNLEVL EKWR
Sbjct: 181 KTAGRAIDHIAAGLDIEVSLHVCGDIRNVLSDLLRFKVDVLDLEFAGRPSNLEVLEEKWR 240

Query: 241 GDKKLGFGCVDTSTEVVESTDTIKNLIERGADIAGEDNLYIDPDCGMRKLPREAAFSKLR 300
           GDK +GFGCVDT+TE VES + I+NLI+RGADI GE+NLYIDPDCGMRKLPR+AAFSKLR
Sbjct: 241 GDKGVGFGCVDTTTERVESMEEIRNLIKRGADIVGEENLYIDPDCGMRKLPRKAAFSKLR 300

Query: 301 NMVKAA 306
           NMV AA
Sbjct: 301 NMVMAA 306


Lambda     K      H
   0.319    0.136    0.389 

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: 383
Number of extensions: 5
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: 309
Length of database: 308
Length adjustment: 27
Effective length of query: 282
Effective length of database: 281
Effective search space:    79242
Effective search space used:    79242
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: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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