Align Alpha-ketoglutaric semialdehyde dehydrogenase; alphaKGSA dehydrogenase; 2,5-dioxovalerate dehydrogenase; EC 1.2.1.26 (characterized)
to candidate WP_078430037.1 BK574_RS21470 aldehyde dehydrogenase family protein
Query= SwissProt::P42236 (488 letters) >NCBI__GCF_002019605.1:WP_078430037.1 Length = 497 Score = 400 bits (1029), Expect = e-116 Identities = 212/481 (44%), Positives = 299/481 (62%), Gaps = 2/481 (0%) Query: 6 EQN-TYLNFINGEWVKSQSGDMVKVENPADVNDIVGYVQNSTAEDVERAVTAANEAKTAW 64 EQN TY NFINGEW S SG+ V P N ++G+ ST EDV AV AA++A +W Sbjct: 15 EQNKTYENFINGEWKSSLSGETYPVSCPGKNNIVLGHFPYSTEEDVNLAVEAAHQAFQSW 74 Query: 65 RKLTGAERGQYLYKTADIMEQRLEEIAACATREMGKTLPEAKGETARGIAILRYYAGEGM 124 ++ G +R L K AD+++ LEE+A + E GK L EA+GE R I R AG+ + Sbjct: 75 SQVPGPDRAAILLKFADLLQDHLEELAFILSAEQGKVLAEARGEVGRAIKETRNVAGDAI 134 Query: 125 RKTGDVIPSTDKDALMFTTRVPLGVVGVISPWNFPVAIPIWKMAPALVYGNTVVIKPATE 184 R G +PS + P+GVV I+PWNFPV PI K+ PAL YG TVV KPA+E Sbjct: 135 RIEGTTLPSEKSNVTAAVKHQPIGVVAAIAPWNFPVVTPIRKIVPALAYGCTVVYKPASE 194 Query: 185 TAVTCAKIIACFEEAGLPAGVINLVTGPGSVVGQGLAEHDGVNAVTFTGSNQVGKIIGQA 244 T T KI+ +AG+P GV+NLV+G GS VG L H V V+FTGS VG + + Sbjct: 195 TPWTSIKIMELLYKAGVPNGVVNLVSGSGSKVGNPLTNHPLVKGVSFTGSTGVGTRLNEM 254 Query: 245 ALARGAKYQLEMGGKNPVIVADDADLEAAAEAVITGAFRSTGQKCTATSRVIVQSGIYER 304 A R K QLE+GGKNP +V D D+ A+ ++ AF +GQ+CT+ SRVIV E Sbjct: 255 AARRLVKTQLELGGKNPAVVLDYEDVNVVAKEIVGAAFACSGQRCTSISRVIVLKEKAEE 314 Query: 305 FKEKLLQRTKDITIGDSLKEDVWMGPIASKNQLDNCLSYIEKGKQEGASLLIGGEKLENG 364 + ++ + +G S + +GP+ +K+QL+ L+YI+ GK EGA+L +GGE L G Sbjct: 315 LVSAIKEQMNALKVGPSWEPTSTIGPLVNKDQLETTLNYIKIGKDEGATLELGGEVLSEG 374 Query: 365 KYQNGYYVQPAIFDNVTSEMTIAQEEIFGPVIALIKVDSIEEALNIANDVKFGLSASIFT 424 + G YV PA+F NVT EM IA+EEIFGPV+++++V+S E+AL +ANDV++GL+ASIFT Sbjct: 375 EMGEGNYVVPALFTNVTPEMKIAKEEIFGPVLSVLEVESFEDALEVANDVEYGLAASIFT 434 Query: 425 ENIGRMLSFIDEIDAGLVRINAESAGVELQAPFGGMKQSSSHSREQGEAAKDFFTAIKTV 484 N+ F++ +++G+V +N +A + PFGG+KQS + G+ K+F+T +K Sbjct: 435 NNLSLANRFVEAVESGMVHVNHGTAS-QAHVPFGGVKQSGYGAYSIGKTNKEFYTNVKVS 493 Query: 485 F 485 + Sbjct: 494 Y 494 Lambda K H 0.315 0.132 0.374 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: 626 Number of extensions: 18 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: 488 Length of database: 497 Length adjustment: 34 Effective length of query: 454 Effective length of database: 463 Effective search space: 210202 Effective search space used: 210202 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 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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