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: A4HJB7
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003677 | DNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.520 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.389 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.413 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.539 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.695 |
DEG_SPOP_SBC_1 | 247 | 251 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 452 | 456 | PF00917 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 306 | 312 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.539 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.483 |
DOC_PP1_RVXF_1 | 417 | 423 | PF00149 | 0.479 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.519 |
DOC_PP2B_LxvP_1 | 280 | 283 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.542 |
DOC_SPAK_OSR1_1 | 421 | 425 | PF12202 | 0.479 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.578 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 206 | 214 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 488 | 496 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.520 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.581 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.518 |
LIG_EVH1_1 | 311 | 315 | PF00568 | 0.592 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.605 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.514 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.403 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.509 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.516 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.516 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.612 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.501 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 518 | 525 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.533 |
LIG_PDZ_Class_2 | 520 | 525 | PF00595 | 0.468 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.497 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.534 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.651 |
LIG_SH3_2 | 28 | 33 | PF14604 | 0.445 |
LIG_SH3_2 | 314 | 319 | PF14604 | 0.644 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.598 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.543 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.574 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.590 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.619 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.628 |
LIG_SUMO_SIM_anti_2 | 437 | 442 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 112 | 118 | PF11976 | 0.524 |
LIG_WRC_WIRS_1 | 122 | 127 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 2 | 7 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 285 | 290 | PF05994 | 0.608 |
LIG_WRC_WIRS_1 | 520 | 525 | PF05994 | 0.468 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.705 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.583 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.676 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.552 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.511 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.517 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.659 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.635 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.771 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.571 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.689 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.618 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.526 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.466 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.739 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.683 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.507 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.473 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.660 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.793 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.601 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.633 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.686 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.700 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.759 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.503 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.616 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.551 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.723 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.466 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.647 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.567 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.664 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.652 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.541 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.584 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.617 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.710 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.632 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.635 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.680 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.501 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.605 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.555 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.591 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.594 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.517 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.507 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.574 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.578 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.506 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.643 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.469 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.491 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.445 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.606 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.694 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.661 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.564 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.539 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.608 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.393 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.608 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.537 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.506 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.510 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.524 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.688 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.509 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.670 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.524 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.645 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.531 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.585 |
MOD_Plk_2-3 | 240 | 246 | PF00069 | 0.699 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.522 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.414 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.349 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.706 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.781 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.684 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.417 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.614 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.519 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.682 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.521 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.511 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.460 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 508 | 513 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 419 | 422 | PF00400 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P654 | Leptomonas seymouri | 40% | 95% |
A0A3S7X4H1 | Leishmania donovani | 61% | 98% |
A4I6R0 | Leishmania infantum | 61% | 98% |
E9B1T2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 99% |
Q4Q6C9 | Leishmania major | 62% | 100% |