GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Thiohalomonas denitrificans HLD2

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_092996902.1 BLP65_RS11095 homoserine O-succinyltransferase

Query= SwissProt::Q3J7P0
         (358 letters)



>NCBI__GCF_900102855.1:WP_092996902.1
          Length = 355

 Score =  535 bits (1379), Expect = e-157
 Identities = 251/355 (70%), Positives = 301/355 (84%), Gaps = 1/355 (0%)

Query: 1   MPLVANSDLPAFERLREEGETVIPRDVALHQDIREMHIGLLNMMPDAALAATERQFFRLI 60
           MPLVAN++LPAF RLR+EG+ V+ RDVA+HQDIRE+H+GLLNMMPDAAL+ATERQFFRL+
Sbjct: 1   MPLVANTELPAFSRLRQEGQNVLERDVAVHQDIRELHVGLLNMMPDAALSATERQFFRLV 60

Query: 61  GESNQIAQFYIHPFTLKEIQRSLEANHYVERYYQTFEQIQAEGLDALIITGANVTQPQLS 120
           GE+NQIAQFY+HPFTLKE++R  +A  +++RYY+ FE +  EGLDALIITGANV   +LS
Sbjct: 61  GEANQIAQFYMHPFTLKELERGPDAAGHIDRYYERFEDLMDEGLDALIITGANVQGTELS 120

Query: 121 LEPFWKPLIKVISWAYENVTSTLCSCLATHAVLDFRYGQKRRRLSSKRWGVYSHRVVNRS 180
            +PFWKPLI+VI WAYENVTSTLCSCL THAV++FRYGQKRR L  KRWGVYSHR V+  
Sbjct: 121 EQPFWKPLIRVIDWAYENVTSTLCSCLTTHAVMEFRYGQKRRPLGFKRWGVYSHR-VSGQ 179

Query: 181 HPLVRGVNTRFDVPHSRFNEISRDQFEAAGLHVLAESEKGGAHLAVSEDLFRIVFCQGHP 240
           HPLV GVNTRFDVPHSRFN I R+QFE+ G  VLAESE+ G HLA SEDLFR+VF QGHP
Sbjct: 180 HPLVAGVNTRFDVPHSRFNAIGREQFESVGCRVLAESEEAGVHLATSEDLFRLVFFQGHP 239

Query: 241 EYDSISLLKEYKREILRFASGQRDNYPPFPENYFSPKIQAILEEYQEQIIIARDKDLPLP 300
           EYD ISLLKEYKRE+  F +G+RD+YPP  +NYF+P+ +AIL+E++ ++  AR++  P+P
Sbjct: 240 EYDVISLLKEYKREVTLFGAGRRDDYPPSIDNYFTPQAEAILDEHRLRVSSARERGQPIP 299

Query: 301 QLPEPLIVDYLDNTWHDTAEAIINNWMGNVYQITHSDRKRPFMEDIAPDDPLGLR 355
           + PE LIVDYLDNTWHDTAEAIIN W+G VYQ+TH DRKRPF E I P+DP GLR
Sbjct: 300 EFPEKLIVDYLDNTWHDTAEAIINKWIGRVYQLTHHDRKRPFKEGIDPNDPFGLR 354


Lambda     K      H
   0.321    0.137    0.416 

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: 500
Number of extensions: 15
Number of successful extensions: 2
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: 358
Length of database: 355
Length adjustment: 29
Effective length of query: 329
Effective length of database: 326
Effective search space:   107254
Effective search space used:   107254
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 (21.9 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