Align Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_007152862.1 MDG893_RS06100 2-hydroxymuconic semialdehyde dehydrogenase
Query= SwissProt::Q9I6M5 (483 letters) >NCBI__GCF_000170835.1:WP_007152862.1 Length = 486 Score = 296 bits (759), Expect = 8e-85 Identities = 171/478 (35%), Positives = 267/478 (55%), Gaps = 11/478 (2%) Query: 14 YVDGAWVDADNGQTIKVNNPATGEIIGSVPKMGAAETRRAIEAADKALPA-WRALTAKER 72 Y++G +V + +G+ NPA G++I V + G E A++AA AL W +T +ER Sbjct: 7 YINGQYVGSASGKLFDNVNPANGQVISKVHEAGREEVDAAVKAAKSALRGPWGKMTLEER 66 Query: 73 ANKLRRWFDLMIENQDDLARLMTIEQGKPLAEAKG-EIAYAASFLEWFGEEAKRIYGDTI 131 L + D + ++ ++ GKP + A +I A+ + F + K + ++ Sbjct: 67 TGILHKVADGINARFEEFLEAECLDTGKPRSLASHIDIPRGAANFKVFADMIKNVPTESF 126 Query: 132 PGHQPDKRIIV---IKQPIGVTAAITPWNFPSAMITRKAGPALAAGCTMVLKPASQTPYS 188 PD + +++P GV I+PWN P ++T K GPALA G T+V+KP+ +TP + Sbjct: 127 EMPTPDGTGALNYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPSEETPTT 186 Query: 189 ALALAELAERAGIPKGVFSVVTGSAGEVGGE-LTSNPIVRKLTFTGSTEIGRQLMAECAQ 247 L ++ + AG+P GVF+VV G G+ G LT +P+V TFTG T G +M A+ Sbjct: 187 TALLGDVMKDAGVPDGVFNVVHGFGGDSAGAFLTEHPMVDGFTFTGETGTGEVIMKAAAK 246 Query: 248 DIKKVSLELGGNAPFIVFDDADLDAAVEGALISKYRNNGQTCVCANRLYVQDGVYDAFVD 307 I+ +SLELGG +VF D D+D A+EG + S + N GQ C+ R+YV+ ++D FV Sbjct: 247 GIRDISLELGGKNAGLVFADCDMDKAIEGTMRSAFANCGQVCLGTERVYVERSIFDEFVG 306 Query: 308 KLKAAVAKLNIGNGLEAGVTTGPLIDAKAVAKVEEHIADAVSKGAKVVSGG----KPHAL 363 +LK A + IG + GPL+ K KV + AV GA +V+GG P AL Sbjct: 307 RLKEAAEGIKIGPPDDIEADMGPLVSLKHREKVLSYYQKAVDDGATLVTGGGVPEMPEAL 366 Query: 364 -GGTFFEPTILVDVPKNALVSKDETFGPLAPVFRFKDEAEVIAMSNDTEFGLASYFYARD 422 GG + +PTI +P+++ V DE FGP + F +E E I ++N +GLAS ++ + Sbjct: 367 AGGAWVQPTIWTGLPEDSAVITDEIFGPCVHLCPFDNEEEAIELANSLPYGLASAIWSEN 426 Query: 423 LARVFRVAEQLEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCL 480 + R RVA Q+E G++ +N+ + + PFGG K SG+GREG + +E Y E+K +C+ Sbjct: 427 ITRAHRVAGQIEAGIIWVNSWFLRDLRTPFGGSKQSGIGREGGVHSLEFYTEMKNICV 484 Lambda K H 0.317 0.135 0.391 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: 623 Number of extensions: 32 Number of successful extensions: 4 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: 483 Length of database: 486 Length adjustment: 34 Effective length of query: 449 Effective length of database: 452 Effective search space: 202948 Effective search space used: 202948 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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