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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HI33
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 38 | 44 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.328 |
DEG_APCC_DBOX_1 | 621 | 629 | PF00400 | 0.416 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.448 |
DOC_MAPK_DCC_7 | 663 | 673 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.540 |
DOC_MAPK_HePTP_8 | 298 | 310 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.366 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.554 |
DOC_PP4_FxxP_1 | 467 | 470 | PF00568 | 0.412 |
DOC_SPAK_OSR1_1 | 205 | 209 | PF12202 | 0.552 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.596 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.476 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 436 | 442 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 622 | 631 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 641 | 649 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 663 | 672 | PF00244 | 0.496 |
LIG_14-3-3_CterR_2 | 695 | 699 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 202 | 219 | PF00022 | 0.455 |
LIG_Actin_WH2_2 | 303 | 321 | PF00022 | 0.272 |
LIG_Actin_WH2_2 | 601 | 616 | PF00022 | 0.575 |
LIG_AP2alpha_1 | 672 | 676 | PF02296 | 0.280 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 575 | 579 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 668 | 672 | PF00533 | 0.438 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.432 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.474 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.520 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.544 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.561 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.446 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.447 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.567 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.446 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.511 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.550 |
LIG_HCF-1_HBM_1 | 101 | 104 | PF13415 | 0.541 |
LIG_LIR_Apic_2 | 240 | 244 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 465 | 470 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 3 | 14 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 507 | 518 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 576 | 582 | PF02991 | 0.440 |
LIG_MLH1_MIPbox_1 | 19 | 23 | PF16413 | 0.415 |
LIG_NRBOX | 8 | 14 | PF00104 | 0.419 |
LIG_PCNA_PIPBox_1 | 327 | 336 | PF02747 | 0.558 |
LIG_PCNA_yPIPBox_3 | 285 | 293 | PF02747 | 0.499 |
LIG_PCNA_yPIPBox_3 | 403 | 412 | PF02747 | 0.496 |
LIG_Pex14_1 | 67 | 71 | PF04695 | 0.480 |
LIG_Pex14_2 | 672 | 676 | PF04695 | 0.280 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.762 |
LIG_SH2_GRB2like | 111 | 114 | PF00017 | 0.768 |
LIG_SH2_GRB2like | 132 | 135 | PF00017 | 0.783 |
LIG_SH2_NCK_1 | 479 | 483 | PF00017 | 0.557 |
LIG_SH2_PTP2 | 6 | 9 | PF00017 | 0.425 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.680 |
LIG_SH2_SRC | 111 | 114 | PF00017 | 0.791 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.463 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.671 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.425 |
LIG_SH3_2 | 543 | 548 | PF14604 | 0.630 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.527 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.567 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.570 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 388 | 394 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 529 | 534 | PF11976 | 0.421 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.548 |
LIG_UBA3_1 | 189 | 197 | PF00899 | 0.446 |
LIG_UBA3_1 | 457 | 463 | PF00899 | 0.521 |
LIG_UBA3_1 | 516 | 524 | PF00899 | 0.548 |
LIG_WRC_WIRS_1 | 502 | 507 | PF05994 | 0.569 |
LIG_WW_3 | 542 | 546 | PF00397 | 0.554 |
MOD_CDC14_SPxK_1 | 30 | 33 | PF00782 | 0.455 |
MOD_CDC14_SPxK_1 | 660 | 663 | PF00782 | 0.336 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.444 |
MOD_CDK_SPxK_1 | 657 | 663 | PF00069 | 0.474 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.411 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.568 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.631 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.564 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.552 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.514 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.464 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.487 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.513 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.558 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.579 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.470 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.530 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.548 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.288 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.489 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.389 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.379 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.581 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.542 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.436 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.369 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.482 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.592 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.458 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.459 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.308 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.296 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.563 |
MOD_N-GLC_1 | 641 | 646 | PF02516 | 0.494 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.444 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.431 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.465 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.533 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.297 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.455 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.552 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.464 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.549 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.553 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.440 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.641 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.354 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.531 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.411 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.430 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.572 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.440 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.482 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.420 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.416 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.399 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.429 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.444 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.340 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.529 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.563 |
MOD_SUMO_for_1 | 192 | 195 | PF00179 | 0.505 |
MOD_SUMO_for_1 | 245 | 248 | PF00179 | 0.572 |
TRG_AP2beta_CARGO_1 | 204 | 213 | PF09066 | 0.332 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.463 |
TRG_DiLeu_LyEn_5 | 211 | 216 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.555 |
TRG_NES_CRM1_1 | 302 | 316 | PF08389 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 606 | 610 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I169 | Leptomonas seymouri | 43% | 100% |
A0A0S4JB89 | Bodo saltans | 25% | 94% |
A0A1X0P251 | Trypanosomatidae | 37% | 100% |
A0A3S7X349 | Leishmania donovani | 80% | 100% |
A0A422P4U2 | Trypanosoma rangeli | 36% | 100% |
A4I5A9 | Leishmania infantum | 80% | 100% |
C9ZQP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 94% |
E9B0K5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q7M7 | Leishmania major | 78% | 97% |