GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_3 in Sinorhizobium meliloti 1021

Align Methionine synthase component, pterin-binding domain (EC:2.1.1.13) (characterized)
to candidate SMc04342 SMc04342 methyltetrahydrofolate:corrinoid/iron-sulfur protein methyltransferase

Query= reanno::Phaeo:GFF1582
         (353 letters)



>FitnessBrowser__Smeli:SMc04342
          Length = 320

 Score =  398 bits (1022), Expect = e-115
 Identities = 218/361 (60%), Positives = 255/361 (70%), Gaps = 55/361 (15%)

Query: 1   MTRTVVESKTKTAILGFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDALAQVMAGA 60
           MTRT+V S T+  I+GFD+PFCVIGERINPTGRKKLAAE+  G+F TV KDAL QV AGA
Sbjct: 1   MTRTIVASATREIIIGFDQPFCVIGERINPTGRKKLAAEMIEGNFDTVIKDALEQVAAGA 60

Query: 61  NILDINAGVVYNSNPNPNETEPPLMTKIVELVQGLTDTPLCIDSSVPGALEAGLQAAEGR 120
            +LD+NAGV   +  +PNETEPPL+ K +E+VQGL D PL IDSSV  A+EAGL+ A+GR
Sbjct: 61  TMLDVNAGV---TAVDPNETEPPLLVKTLEIVQGLVDVPLSIDSSVTAAIEAGLRVAKGR 117

Query: 121 PLLNSVTGEEERLEHVLPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVERAADFGI 180
           PL+NSVTGEEE+LE +LPL KKY+VPVVAISND+TGIS DPDVRFAVAKKIVERAAD+GI
Sbjct: 118 PLVNSVTGEEEKLEAILPLCKKYDVPVVAISNDETGISMDPDVRFAVAKKIVERAADYGI 177

Query: 181 PAHDIVVDPLVMPIGAMATAGQQVFALVRRLREELGVNTTCGASNVSFGLPNRHGINNAF 240
             HDIVVDPLVMPIGA+ +AGQQVFAL+RRLREEL VNTTCG SN+SFGLP+RHGIN  F
Sbjct: 178 KPHDIVVDPLVMPIGALGSAGQQVFALLRRLREELKVNTTCGLSNISFGLPHRHGINAGF 237

Query: 241 LPMAMGAGMTSAIMNPVALPITQKKIAEKKAEVEAAGIILPEGMEDEAFVQMFGLGSTKP 300
           +PM +GAGMTSAIMNP                                          +P
Sbjct: 238 IPMVIGAGMTSAIMNP-----------------------------------------CRP 256

Query: 301 RAGKEMEAIRAANLLTNNDPHGGEWIKANKE--PAKEGE------EGRGRGGRAGGRRRR 352
              +EMEA+RAAN+L   DP+   WI   ++  PA+ G          G GGR GGR  R
Sbjct: 257 ---QEMEAVRAANVLNGTDPNCTNWIMTYRDHKPAEGGHAVAAAAAPAGAGGRRGGRAAR 313

Query: 353 A 353
           A
Sbjct: 314 A 314


Lambda     K      H
   0.315    0.134    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: 387
Number of extensions: 10
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: 353
Length of database: 320
Length adjustment: 28
Effective length of query: 325
Effective length of database: 292
Effective search space:    94900
Effective search space used:    94900
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: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 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