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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HKJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.492 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.275 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.418 |
DEG_SCF_FBW7_1 | 201 | 206 | PF00400 | 0.548 |
DEG_SCF_FBW7_1 | 70 | 76 | PF00400 | 0.571 |
DOC_CKS1_1 | 70 | 75 | PF01111 | 0.597 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 31 | 40 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 404 | 410 | PF00134 | 0.371 |
DOC_MAPK_MEF2A_6 | 336 | 345 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 493 | 499 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 253 | 256 | PF13499 | 0.506 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.429 |
DOC_USP7_MATH_2 | 241 | 247 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 322 | 329 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 52 | 62 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 273 | 290 | PF00022 | 0.313 |
LIG_BIR_III_4 | 195 | 199 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.475 |
LIG_Clathr_ClatBox_1 | 19 | 23 | PF01394 | 0.328 |
LIG_deltaCOP1_diTrp_1 | 243 | 251 | PF00928 | 0.489 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.499 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.565 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.488 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.607 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.529 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.521 |
LIG_Integrin_RGD_1 | 208 | 210 | PF01839 | 0.564 |
LIG_MYND_1 | 237 | 241 | PF01753 | 0.368 |
LIG_MYND_1 | 445 | 449 | PF01753 | 0.514 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.469 |
LIG_PDZ_Class_1 | 534 | 539 | PF00595 | 0.462 |
LIG_REV1ctd_RIR_1 | 495 | 505 | PF16727 | 0.564 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.577 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.493 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.328 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.493 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.405 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.530 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.508 |
LIG_SH3_CIN85_PxpxPR_1 | 252 | 257 | PF14604 | 0.575 |
LIG_SUMO_SIM_anti_2 | 339 | 346 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 74 | 81 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 143 | 152 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.401 |
LIG_UBA3_1 | 19 | 25 | PF00899 | 0.337 |
MOD_CDK_SPxxK_3 | 315 | 322 | PF00069 | 0.562 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.604 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.602 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.755 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.595 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.581 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.402 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.346 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.530 |
MOD_DYRK1A_RPxSP_1 | 257 | 261 | PF00069 | 0.429 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.717 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.549 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.427 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.523 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.536 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.643 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.359 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.517 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.493 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.452 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.506 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.622 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.567 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.486 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.569 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.554 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.546 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.362 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.660 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.515 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.695 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.424 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.650 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.545 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.568 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.569 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.587 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.527 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.493 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.531 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.316 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.337 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.351 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.472 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.312 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.427 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.444 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.423 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.358 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.559 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.590 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.465 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.508 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.565 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.413 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.504 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.583 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.431 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.706 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.538 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.623 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.509 |
TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.548 |
TRG_DiLeu_LyEn_5 | 333 | 338 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.481 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXU5 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IL67 | Leishmania donovani | 70% | 99% |
A4I830 | Leishmania infantum | 70% | 99% |
E9B2Y8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 99% |
Q4Q568 | Leishmania major | 68% | 100% |