GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpE in Sinorhizobium medicae WSM419

Align Anthranilate synthase component 1 2; EC 4.1.3.27; Anthranilate synthase component I 2 (uncharacterized)
to candidate YP_001328350.1 Smed_2685 aminodeoxychorismate synthase

Query= curated2:Q9HS66
         (488 letters)



>NCBI__GCF_000017145.1:YP_001328350.1
          Length = 385

 Score =  181 bits (460), Expect = 3e-50
 Identities = 119/327 (36%), Positives = 173/327 (52%), Gaps = 17/327 (5%)

Query: 154 DLRLIAAVPVDEYTP---DGAFEA-GRDRVQSLAAAIRDGDPAVGPPPADSPAPFESVAG 209
           + +L    P +  TP    G F+A   D   ++A    + +P +  P A    P      
Sbjct: 66  ETKLAPFAPENRETPLMSFGVFDAPAEDHALAVARRRSENEPFLLEPRAGWDFP------ 119

Query: 210 RAAFESRVRRIQDAIRDGDTFQANVSHRLDAPAAVHPVAVFEALRDTNPAPYSGIVEFPG 269
             A+  R  R+   +R GD +QAN++  + A  +  P+A F +L +  P  Y  +V   G
Sbjct: 120 --AYRQRFERLHRHLRQGDCYQANLTMPIQARWSGDPLAAFWSLIERQPVRYGALVALDG 177

Query: 270 VDLVSASPELLLARRGRE-LTTEPIAGTRPRGATPAEDDAARAALRADDKERAEHAMLVD 328
             L+S SPEL         + T P+ GT  RGA+P EDDA  AA+RAD+K +AE+ M+VD
Sbjct: 178 PVLLSRSPELFFRVDAEGWIETHPMKGTARRGASPKEDDAIIAAMRADEKTQAENRMIVD 237

Query: 329 LERNDLGKVSEYGSVAVPDYRRVDAYSEVLHLVSEVTGRLRDSCSLRDAIAAVFPGGTIT 388
           L RND+ +V+E G++ VP    ++ Y  V  +VS V  +L     + D  AA+FP G++T
Sbjct: 238 LLRNDISRVTEVGTLDVPKLFDIETYPTVHQMVSHVRAKLLTDIGIADIFAALFPCGSVT 297

Query: 389 GAPKPRTMALIDTVEATRRGPYTGSLAAIGFDGDATLSITIRTL-VRRAATYHLRVGAGI 447
           GAPK R M ++  +E+  R  Y G++  I  DG    S+ IRT+ +         VG GI
Sbjct: 298 GAPKMRAMEILHDLESGPRDAYCGAIGYIAPDGAMRFSVAIRTISLFPGGEAVFNVGGGI 357

Query: 448 VHDSTPAAEYDETLAKARALVTALGDA 474
           V DST  AEY+E L KAR    A+GDA
Sbjct: 358 VFDSTAEAEYEECLLKAR---FAVGDA 381


Lambda     K      H
   0.317    0.135    0.397 

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: 464
Number of extensions: 25
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: 488
Length of database: 385
Length adjustment: 32
Effective length of query: 456
Effective length of database: 353
Effective search space:   160968
Effective search space used:   160968
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: 51 (24.3 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