Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4I1P7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.332 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.613 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.325 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.419 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.367 |
DOC_CDC14_PxL_1 | 437 | 445 | PF14671 | 0.575 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.367 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.325 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 409 | 418 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.325 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.704 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.234 |
DOC_USP7_UBL2_3 | 282 | 286 | PF12436 | 0.574 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.385 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.214 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 485 | 491 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 353 | 371 | PF00022 | 0.325 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.593 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.391 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.253 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.765 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.466 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.587 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.329 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.333 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.400 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.665 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.638 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.554 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 309 | 319 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 356 | 364 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 572 | 580 | PF02991 | 0.751 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.706 |
LIG_MYND_1 | 379 | 383 | PF01753 | 0.454 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.577 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.581 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.574 |
LIG_SH2_GRB2like | 277 | 280 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 297 | 301 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.360 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.385 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.325 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.325 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.564 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.727 |
LIG_SH3_4 | 400 | 407 | PF00018 | 0.601 |
LIG_TYR_ITSM | 307 | 314 | PF00017 | 0.366 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.363 |
LIG_WW_1 | 269 | 272 | PF00397 | 0.668 |
MOD_CDC14_SPxK_1 | 482 | 485 | PF00782 | 0.637 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.307 |
MOD_CDK_SPK_2 | 479 | 484 | PF00069 | 0.588 |
MOD_CDK_SPxK_1 | 159 | 165 | PF00069 | 0.258 |
MOD_CDK_SPxK_1 | 479 | 485 | PF00069 | 0.632 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.385 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.307 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.537 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.700 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.667 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.569 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.466 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.739 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.613 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.385 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.651 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.331 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.342 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.743 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.569 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.637 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.544 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.561 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.575 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.587 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.658 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.366 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.360 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.431 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.727 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.676 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.703 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.728 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.677 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.724 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.530 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.680 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.665 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.402 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.293 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.765 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.546 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.357 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.280 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.662 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.610 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.616 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.627 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.625 |
MOD_N-GLC_2 | 229 | 231 | PF02516 | 0.526 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.385 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.533 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.758 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.605 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.357 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.640 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.652 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.546 |
MOD_NEK2_2 | 486 | 491 | PF00069 | 0.586 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.539 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.307 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.567 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.649 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.658 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.392 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.616 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.587 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.298 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.363 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.715 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.385 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.367 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.498 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.214 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.677 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.377 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.697 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.683 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.703 |
MOD_SUMO_rev_2 | 393 | 401 | PF00179 | 0.600 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_2 | 571 | 577 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 438 | 443 | PF01217 | 0.639 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 535 | 538 | PF00400 | 0.647 |
TRG_NES_CRM1_1 | 118 | 133 | PF08389 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W2 | Leptomonas seymouri | 55% | 97% |
A0A0S4JI27 | Bodo saltans | 24% | 81% |
A0A3S7WZA6 | Leishmania donovani | 99% | 100% |
A4HEA1 | Leishmania braziliensis | 77% | 98% |
C9ZK98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AXT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
Q4Q9P0 | Leishmania major | 93% | 99% |