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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
Related structures:
AlphaFold database: Q4Q2S7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 234 | 240 | PF00089 | 0.467 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.572 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.448 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.488 |
DEG_APCC_DBOX_1 | 422 | 430 | PF00400 | 0.522 |
DOC_ANK_TNKS_1 | 412 | 419 | PF00023 | 0.521 |
DOC_CKS1_1 | 64 | 69 | PF01111 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 413 | 421 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 442 | 452 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 413 | 421 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 445 | 454 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.537 |
DOC_MAPK_NFAT4_5 | 414 | 422 | PF00069 | 0.488 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 358 | 365 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 467 | 476 | PF00244 | 0.414 |
LIG_APCC_ABBA_1 | 450 | 455 | PF00400 | 0.581 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BIR_III_2 | 320 | 324 | PF00653 | 0.636 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.469 |
LIG_CSL_BTD_1 | 532 | 535 | PF09270 | 0.394 |
LIG_EH1_1 | 43 | 51 | PF00400 | 0.553 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.447 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.457 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.447 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.391 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.678 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.482 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.401 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.445 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.548 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.631 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.426 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.559 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.687 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.639 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.548 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.433 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.597 |
LIG_HCF-1_HBM_1 | 246 | 249 | PF13415 | 0.559 |
LIG_MLH1_MIPbox_1 | 450 | 454 | PF16413 | 0.467 |
LIG_Pex14_2 | 376 | 380 | PF04695 | 0.464 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.667 |
LIG_SH2_GRB2like | 183 | 186 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.709 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.535 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.488 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.640 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.616 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.407 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.547 |
LIG_UBA3_1 | 49 | 56 | PF00899 | 0.435 |
LIG_WW_3 | 355 | 359 | PF00397 | 0.624 |
LIG_WW_3 | 464 | 468 | PF00397 | 0.592 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.552 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.667 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.377 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.609 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.607 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.493 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.640 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.623 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.553 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.401 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.483 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.722 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.519 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.634 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.507 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.556 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.260 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.426 |
MOD_GlcNHglycan | 3 | 7 | PF01048 | 0.602 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.655 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.422 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.580 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.371 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.675 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.459 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.383 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.564 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.672 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.547 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.461 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.449 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.332 |
MOD_LATS_1 | 305 | 311 | PF00433 | 0.634 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.571 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.501 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.370 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.498 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.458 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.546 |
MOD_NEK2_2 | 526 | 531 | PF00069 | 0.370 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.539 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.582 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.439 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.591 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.446 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.528 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.562 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.491 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.558 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.507 |
MOD_Plk_1 | 526 | 532 | PF00069 | 0.354 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.418 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.484 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.571 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.564 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.710 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.547 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.473 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.543 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.673 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.727 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 513 | 515 | PF00400 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 71 | 76 | PF00026 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E9 | Leptomonas seymouri | 68% | 94% |
A0A0S4JQH6 | Bodo saltans | 33% | 100% |
A0A1X0P9Q5 | Trypanosomatidae | 43% | 100% |
A0A3Q8IUQ4 | Leishmania donovani | 93% | 99% |
A0A3R7L5W7 | Trypanosoma rangeli | 42% | 100% |
A4HAY5 | Leishmania braziliensis | 85% | 99% |
A4IA44 | Leishmania infantum | 94% | 98% |
C9ZM56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B558 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BKS0 | Trypanosoma cruzi | 43% | 100% |